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    1. Ilan, T; Shohat, T; Tobar, A; Magal, N; Yahav, M; Halpern, GJ; Rechavi, G; Shohat, M
      Autosomal dominant nephritis with renal failure of non-alport type: Clinical and molecular studies

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Bykhovskaya, Y; Yang, HY; Taylor, K; Hang, T; Tun, RYM; Estivill, X; Casano, RAMS; Majamaa, K; Shohat, M; Fischel-Ghodsian, N
      Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

      GENETICS IN MEDICINE
    3. Bar-Hava, I; Yitzhak, M; Krissi, H; Shohat, M; Shalev, J; Czitron, B; Ben-Rafael, Z; Orvieto, R
      Triple-test screening in in vitro fertilization pregnancies

      JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
    4. Toudjarska, I; Kilpatrick, MW; Lembessis, P; Carra, S; Harton, GL; Sisson, ME; Black, SH; Stern, HJ; Gelman-Kohan, Z; Shohat, M; Tsipouras, P
      Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Tanamy, MG; Magal, N; Halpern, GJ; Jaber, L; Shohat, M
      Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Udler, Y; Kauschansky, A; Yeshaya, J; Freedman, J; Barkai, U; Tobar, A; Okon, E; Halpern, GJ; Shohat, M; Legum, C
      Phenotypic expression of tissue mosaicism in a 45,X/46,X,dicY(q11.2) female

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Senecky, Y; Halpern, GJ; Inbar, D; Attias, J; Shohat, M
      Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) insiblings

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Halpern, GJ; Mimouni, A; Shohat, M
      E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients - Reply

      PEDIATRICS
    9. Toledano-Alhadef, H; Basel-Vanagaite, L; Magal, N; Davidov, B; Ehrlich, S; Drasinover, V; Taub, E; Halpern, GJ; Ginott, N; Shohat, M
      Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel

      AMERICAN JOURNAL OF HUMAN GENETICS
    10. Shohat, M; Hodak, E; Sredni, B; Shohat, B; Sredni, D; David, M
      Cytokine profile of patients with mycosis fungoides and the immunomodulatory effect of AS101

      ACTA DERMATO-VENEREOLOGICA
    11. Shohat, M
      The future of genetics: Where are we going in the next forty years?

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    12. Falik-Zaccai, TC; Shachak, E; Abeliovitch, D; Lerer, I; Shefer, R; Carmi, R; Ries, L; Friedman, M; Shohat, M; Borochowitz, Z
      Achondroplasia in diverse Jewish and Arab populations in Israel: Clinical and molecular characterization

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    13. Shohat, T; Green, MS; Nakar, O; Ballin, A; Duvdevani, P; Cohen, A; Shohat, M
      Gender differences in the reactogenicity of measles-mumps-rubella vaccine

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    14. Lotem, Y; Barak, A; Mussaffi, H; Shohat, M; Wilschanski, M; Sivan, Y; Blau, H
      Reaching the diagnosis of cystic fibrosis - the limits of the spectrum

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    15. Jaber, L; Eisenstein, B; Shohat, M
      Blood pressure measurements in Israeli Arab children and adolescents

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    16. Stoffman, N; Magal, N; Shohat, T; Lotan, R; Koman, S; Oron, A; Danon, Y; Halpern, GJ; Lifshitz, Y; Shohat, M
      Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

      EUROPEAN JOURNAL OF HUMAN GENETICS
    17. Sobe, T; Vreugde, S; Shahin, H; Berlin, M; Davis, N; Kanaan, M; Yaron, Y; Orr-Urtreger, A; Frydman, M; Shohat, M; Avraham, KB
      The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

      HUMAN GENETICS
    18. Udler, Y; Halpern, GJ; Lachman, RS; Rimoin, DL; Shohat, M
      Pathological fractures in spondyloenchondrodysplasia: case report

      PEDIATRIC RADIOLOGY
    19. Drasinover, V; Ehrlich, S; Magal, N; Taub, E; Libman, V; Shohat, T; Halpern, GJ; Shohat, M
      Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Molad, Y; Gal, E; Magal, N; Sulkes, J; Mukamel, M; Weinberger, A; Lalazari, S; Shohat, M
      Renal outcome and vascular morbidity in systemic lupus erythematosus (SLE): Lack of association with the angiotensin-converting enzyme gene polymorphism

      SEMINARS IN ARTHRITIS AND RHEUMATISM
    21. Mimouni, A; Magal, N; Stoffman, N; Shohat, T; Minasian, A; Krasnov, M; Halpern, GJ; Rotter, JI; Fischel-Ghodsian, N; Danon, YL; Shohat, M
      Familial Mediterranean fever: Effects of genotype and ethnicity on inflammatory attacks and amyloidosis

      PEDIATRICS
    22. Cohn, DH; Shohat, T; Yahav, M; Ilan, T; Rechavi, G; King, L; Shohat, M
      A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. Bykhovskaya, Y; Estivill, X; Taylor, K; Hang, T; Hamon, M; Casano, RAMS; Yang, HY; Rotter, JI; Shohat, M; Fischel-Ghodsian, N
      Candidate locus for a nuclear modifier gene for maternally inherited deafness

      AMERICAN JOURNAL OF HUMAN GENETICS
    24. Michaelovsky, E; Frisch, A; Rockah, R; Peleg, L; Magal, N; Shohat, M; Weizman, R
      A novel allele in the promoter region of the human serotonin transporter gene

      MOLECULAR PSYCHIATRY
    25. Horowitz, M; Pasmanik-Chor, M; Borochowitz, Z; Falik-Zaccai, T; Heldmann, K; Carmi, R; Parvari, R; Beit-Or, H; Goldman, B; Peleg, L; Levy-Lahad, E; Renbaum, P; Legum, S; Shomrat, R; Yeger, H; Benbenisti, D; Navon, R; Dror, V; Shohat, M; Magal, N; Navot, N; Eyal, N
      Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewishpopulation (vol 12, pg 240, 1998)

      HUMAN MUTATION
    26. Shohat, M; Ben Amitai, D; Shohat, B; Mosberg, R; Narinski, R; Klein, T; Okon, E; Roizman, P; Cowan, EP; Alexander, R; David, M
      Atopic dermatitis and HTLV-1-associated myelopathy: Associated or coincidental disorders?

      DERMATOLOGY
    27. Shohat, M; Magal, N; Shohat, T; Chen, X; Dagan, T; Mimouni, A; Danon, Y; Lotan, R; Ogur, G; Sirin, A; Schlezinger, M; Halpern, GJ; Schwabe, A; Kastner, D; Rotter, JI; Fischel-Ghodsian, N
      Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

      EUROPEAN JOURNAL OF HUMAN GENETICS
    28. Yeshaya, J; Shalgi, R; Shohat, M; Avivi, L
      FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes

      HUMAN GENETICS
    29. Shohat, M; Fischel-Ghodsian, N; Legum, C; Halpern, GJ
      Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G

      AMERICAN JOURNAL OF OTOLARYNGOLOGY
    30. Sobe, T; Erlich, P; Berry, A; Korostichevsky, M; Vreugde, S; Avraham, KB; Bonne-Tanir, B; Shohat, M
      High frequency of the deafness-associated 167delT mutation in the connexin26 (GJB2) gene in Israeli Ashkenazim

      AMERICAN JOURNAL OF MEDICAL GENETICS
    31. Amir, A; Wolf, Y; Ezra, Y; Shohat, M; Sher, C; Hauben, DJ
      Pharyngeal flap for velopharyngeal incompetence in patients with myotonic dystrophy

      ANNALS OF PLASTIC SURGERY
    32. Carmi, D; Shohat, M; Metzker, A; Dickerman, Z
      Growth, puberty, and endocrine functions in patients with sporadic or familial neurofibromatosis type 1: A longitudinal study

      PEDIATRICS
    33. Mager, A; Lalezari, S; Shohat, T; Birnbaum, Y; Adler, Y; Magal, N; Shohat, M
      Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease

      CIRCULATION
    34. Shohat, M; Hodak, E; Hannig, H; Bodemer, W; David, M; Shohat, B
      Evidence for the cofactor role of human T-cell lymphotropic virus type 1 in mycosis fungoides and Sezary syndrome

      BRITISH JOURNAL OF DERMATOLOGY
    35. SHOHAT M; HODAK E; SREDNI B; SREDNI D; DAVID M; SHOHAT B
      IMMUNOMODULATION OF CYTOKINE PRODUCTION IN MYCOSIS-FUNGOIDES BY AS-101

      European cytokine network
    36. SHOHAT M; BENAMITAI D; SHOHAT B; SREDNI D; SREDNI B; DAVID M
      CYTOKINE PROFILE IN ATOPIC-DERMATITIS AND THE IMMUNOMODULATORY EFFECTOF AS-101

      European cytokine network
    37. Shohat, M; Lotan, R; Magal, N; Danon, Y; Ogur, G; Tokguz, G; Schlezinger, M; Schwabe, A; Halpern, G; Fischel-Ghodsian, N; Kastner, D; Shohat, T; Rotter, JI
      Amyloidosis in familial Mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus

      MOLECULAR GENETICS AND METABOLISM
    38. HOROWITZ M; PASMANIKCHOR M; BOROCHOWITZ Z; FALIKZACCAI T; HELDMANN K; CARMI R; PARVARI R; BEITOR H; GOLDMAN B; PELEG L; LEVYLAHAD E; RENBAUM P; LEGUM S; SHOMRAT R; YEGER H; BENBENISTI D; NAVON R; DROR V; SHOHAT M; MAGAL N; NAVOT N; EYAL N
      PREVALENCE OF GLUCOCEREBROSIDASE MUTATIONS IN THE ISRAELI ASHKENAZI JEWISH POPULATION

      Human mutation
    39. CHEN XG; FISCHELGHODSIAN N; CERCEK A; HAMON M; OGUR G; LOTAN R; DANON Y; SHOHAT M
      ASSESSMENT OF PYRIN GENE-MUTATIONS IN TURKS WITH FAMILIAL MEDITERRANEAN FEVER (FMF)

      Human mutation
    40. Propheta, O; Magal, N; Shohat, M; Eyal, N; Navot, N; Horowitz, M
      A benign polymorphism in the aspartoacylase gene may cause misinterpretation of Canavan gene testing

      EUROPEAN JOURNAL OF HUMAN GENETICS
    41. YESHAYA J; SHALGI R; SHOHAT M; AVIVI L
      REPLICATION TIMING OF THE VARIOUS FMR1 ALLELES DETECTED BY FISH - INFERENCES REGARDING THEIR TRANSCRIPTIONAL STATUS

      Human genetics
    42. BARHAVA I; YITZHAK M; ORVIETO R; CZITRON B; BENRAFAEL Z; SHOHAT M
      A DIFFERENT TRIPLE-TEST NOMOGRAM SHOULD BE DESIGNED FOR IN-VITRO FERTILIZATION PREGNANCIES

      Human reproduction (Oxford. Print)
    43. ACHIRON A; BARAK Y; MAGAL N; SHOHAT M; COHEN M; BARAR R; GADOTH N
      ABNORMAL LIVER TEST-RESULTS IN MYOTONIC-DYSTROPHY

      Journal of clinical gastroenterology
    44. WILKIN DJ; MORTIER GR; JOHNSON CL; JONES MC; DEPAEPE A; SHOHAT M; WILDIN RS; FALK RE; COHN DH
      CORRELATION OF LINKAGE DATA WITH PHENOTYPE IN 8 FAMILIES WITH STICKLER-SYNDROME

      American journal of medical genetics
    45. BYKHOVSKAYA Y; SHOHAT M; EHRENMAN K; JOHNSON D; HAMON M; CANTOR RM; AOUIZERAT B; BU XD; ROTTER JI; JABER L; FISCHELGHODSIAN N
      EVIDENCE FOR COMPLEX NUCLEAR INHERITANCE IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION

      American journal of medical genetics
    46. KAUSCHANSKY A; SHOHAT M; FRYDMAN M; ROSLER A; GREENBAUM E; SIROTA L
      SYNDROME OF ALOPECIA TOTALIS AND 17B-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY

      American journal of medical genetics
    47. GORSKY M; BUKAI A; SHOHAT M
      GENETIC INFLUENCE ON THE PREVALENCE OF TORUS PALATINUS

      American journal of medical genetics
    48. Udler, Y; Halpern, GJ; Shohat, M; Cohen, D
      Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. WARNER LE; SHOHAT M; SHORER Z; LUPSKI JR
      MULTIPLE DE-NOVO MPZ (P-0) POINT MUTATIONS IN A SPORADIC DEJERINE-SOTTAS CASE

      Human mutation
    50. ZELANTE L; GASPARINI P; ESTIVILL X; MELCHIONDA S; DAGRUMA L; GOVEA N; MILA M; DELLAMONICA M; LUTFI J; SHOHAT M; MANSFIELD E; DELGROSSO K; RAPPAPORT E; SURREY S; FORTINA P
      CONNEXIN26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON-SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS

      Human molecular genetics
    51. BALOW JE; SHELTON DA; ORSBORN A; MANGELSDORF M; AKSENTIJEVICH I; BLAKE T; SOOD R; GARDNER D; LIU R; PRAS E; LEVY EN; CENTOLA M; DENG ZM; ZAKS N; WOOD G; CHEN XG; RICHARDS N; SHOHAT M; LIVNEH A; PRAS M; DOGGETT NA; COLLINS FS; LIU PP; ROTTER JI; FISCHELGHODSIAN N; GUMUCIO D; RICHARDS RI; KASTNER DL
      A HIGH-RESOLUTION GENETIC-MAP OF THE FAMILIAL MEDITERRANEAN FEVER CANDIDATE REGION ALLOWS IDENTIFICATION OF HAPLOTYPE-SHARING AMONG ETHNIC-GROUPS

      Genomics
    52. SOOD R; BLAKE T; AKSENTIJEVICH I; WOOD G; CHEN X; GARDNER D; SHELTON DA; MANGELSDORF M; ORSBORN A; PRAS E; BALOW JE; CENTOLA M; DENG ZM; ZAKS N; CHEN XG; RICHARDS N; FISCHELGHODSIAN N; ROTTER JI; PRAS M; SHOHAT M; DEAVEN LL; GUMUCIO DL; CALLEN DF; RICHARDS RI; COLLINS FS; LIU PP; KASTNER DL; DOGGETT NA
      CONSTRUCTION OF A 1-MB RESTRICTION-MAPPED COSMID CONTIG CONTAINING THE CANDIDATE REGION FOR THE FAMILIAL MEDITERRANEAN FEVER LOCUS (MEFV) ON CHROMOSOME 16P13.3

      Genomics
    53. SHER C; SHOHAT M
      CONGENITAL DEFICIENCY OF AFP AND DOWN-SYNDROME SCREENING

      Prenatal diagnosis
    54. UDLER Y; HALPERN GJ; SHER C; DAVIDOVITZ M; SHOHAT M
      FURTHER DELINEATION OF CEREBRO-OSTEO-NEPHROSIS SYNDROME

      American journal of medical genetics
    55. MORCOHEN R; MAGAL N; GADOTH N; SHOHAT T; SHOHAT M
      CORRELATION BETWEEN THE INCIDENCE OF MYOTONIC-DYSTROPHY IN DIFFERENT GROUPS IN ISRAEL AND THE NUMBER OF CTG TRINUCLEOTIDE REPEATS IN THE MYOTONIN GENE

      American journal of medical genetics
    56. JABER L; SHOHAT T; ROTTER JI; SHOHAT M
      CONSANGUINITY AND COMMON ADULT DISEASES IN ISRAELI ARAB COMMUNITIES

      American journal of medical genetics
    57. INBAR D; HALPERN GJ; WEITZ R; SADEH M; SHOHAT M
      AGENESIS OF THE CORPUS-CALLOSUM IN A MOTHER AND SON

      American journal of medical genetics
    58. AKSENTIJEVICH I; CENTOLA M; DENG ZM; SOOD R; BALOW JE; WOOD G; ZAKS N; MANSFIELD E; CHEN X; EISENBERG S; VEDULA A; SHAFRAN N; RABEN N; PRAS E; PRAS M; KASTNER DL; BLAKE T; BAXEVANIS AD; ROBBINS C; KRIZMAN D; COLLINS FS; LIU PP; CHEN XG; SHOHAT M; HAMON M; KAHAN T; CERCEK A; ROTTER JI; FISCHELGHODSIAN N; RICHARDS N; SHELTON DA; GUMUCIO D; YOKOYAMA Y; MANGELSDORF M; ORSBORN A; RICHARDS RI; RICKE DO; BUCKINGHAM JM; MOYZIS RK; DEAVEN LL; DOGGETT NA
      ANCIENT MISSENSE MUTATIONS IN A NEW MEMBER OF THE RORET GENE FAMILY ARE LIKELY TO CAUSE FAMILIAL MEDITERRANEAN FEVER

      Cell
    59. JABER L; MERLOB P; GABRIEL R; SHOHAT M
      EFFECTS OF CONSANGUINEOUS MARRIAGE ON REPRODUCTIVE OUTCOME IN AN ARABCOMMUNITY IN ISRAEL

      Journal of Medical Genetics
    60. MARKITZIU A; SHOHAT M; BEERI E; BONE A; ZALKIND M
      DENTAL MANIFESTATIONS OF BULIMIA-NERVOSA

      Journal of dental research
    61. JABER L; NAHMANI A; SHOHAT M
      SPEECH DISORDERS IN ISRAELI ARAB CHILDREN

      Israel journal of medical sciences
    62. SHOHAT M; LOTAN R; MAGAL N; SHOHAT T; FISCHELGHODSIAN N; ROTTER JI; JABER L
      A GENE FOR ARTHROGRYPOSIS MULITPLEX CONGENITA NEUROPATHIC TYPE IS LINKED TO D5S394 ON CHROMOSOME 5QTER

      American journal of human genetics
    63. LOTAN R; MAGAL N; SHOHAT T; FISCHELGHODSIAN N; ROTTER JI; JABER L; SHOHAT M
      MAPPING OF A GENE FOR MILD ARTHROGRYPOSIS MULTIPLEX CONGENITA NEUROPATHIC TYPE BETWEEN D5S425 AND D5S2108 ON CHROMOSOME 5QTER

      American journal of human genetics
    64. SHOHAT M; LOTAN R; MAGAL N; OGUR G; TOKGUZ G; SCHWABE A; FISCHELGHODSIAN N; KASTNER D; ROTTER JI; SCHLEZINGER M; DANON Y
      AMYLOIDOSIS IN FMF IS ASSOCIATED WITH A SPECIFIC CORE HAPLOTYPE IN THE MEFV LOCUS

      American journal of human genetics
    65. LEV D; HAFTEL L; HURI Z; MANDELBERG A; BENYEHUDA Y; RIMOIN D; LACHMAN R; SHOHAT M
      A DISTINCT SKELETAL DYSPLASIA WITH OPTIC ATROPHY, KINKY FRAGILE HAIR AND UNUSUAL FACE - A NEW AUTOSOMAL RECESSIVE SYNDROME

      American journal of human genetics
    66. YESHAYA J; SHALGI R; SHOHAT M; AVIVI L
      REPLICATION TIMING OF THE VARIOUS FMR1 ALLELES DETECTED BY FISH

      American journal of human genetics
    67. DAGAN T; LOTAN R; DANON Y; MAGAL N; OGUR G; TOKGUZ G; SCHWABE A; FISCHELGHODSIAN N; ROTTER JI; SCHLEZINGER M; HALPERN GJ; SHOHAT M
      THE VARIOUS FMF CORE HAPLOTYPES IN THE MEFV LOCUS AND THEIR CORRELATION WITH FMF SYMPTOMS

      American journal of human genetics
    68. DENG Z; AKSENTIJEVICH I; BALOW JE; BLAKE T; CENTOLA M; CHEN X; COLLINS FS; DOGGETT N; FISCHELGHODSIAN N; GUMUCIO D; LIU P; PRAS E; PRAS M; RICHARDS N; RICHARDS RI; RICKE DO; ROTTER JI; SHOHAT M; SOOD R; WOOD G; YOKOYAMA Y; ZAKS N; KASTNER DL
      IDENTIFICATION OF FMF POSITIONAL CANDIDATE GENES WITHIN A 115-KB INTERVAL DEFINED BY HISTORICAL RECOMBINANTS

      American journal of human genetics
    69. BYKHOVSKAYA Y; EHRENMAN K; JOHNSON D; HAMON M; CANTOR R; TAYLOR K; BU X; JABER L; ROTTER JI; SHOHAT M; FISCHELGHODSIAN N
      LACK OF EVIDENCE FOR LINKAGE TO A NUCLEAR LOCUS IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION

      American journal of human genetics
    70. LEVYLAHAD E; CATANE R; EISENBERG S; KAUFMAN B; HORNREICH G; LISHINSKY E; SHOHAT M; WEBER BL; BELLER U; LAHAD A; HALLE D
      FOUNDER BRCA1 AND BRCA2 MUTATIONS IN ASHKENAZI JEWS IN ISRAEL - FREQUENCY AND DIFFERENTIAL PENETRANCE IN OVARIAN-CANCER AND IN BREAST-OVARIAN CANCER FAMILIES

      American journal of human genetics
    71. BRAVERMAN I; JABER L; LEVI H; ADELMAN C; ARONS KS; FISCHELGHODSIAN N; SHOHAT M; ELIDAN J
      AUDIOVESTIBULAR FINDINGS IN PATIENTS WITH DEAFNESS CAUSED BY A MITOCHONDRIAL SUSCEPTIBILITY MUTATION AND PRECIPITATED BY AN INHERITED NUCLEAR MUTATION OR AMINOGLYCOSIDES

      Archives of otolaryngology, head & neck surgery
    72. SHOHAT M; HARDY B; MANNHEIMER S; FISCH B; SHOHAT B
      A NEW METHOD FOR ISOLATION OF HUMAN ANTISPERM ANTIBODIES

      Andrologia
    73. SOOD R; AKSENTIJEVICH I; ALTHERR M; APOSTOLOU S; BALOW JE; BLAKE T; CALLEN DF; CENTOLA M; CHEN X; CHEN X; COLLINS FS; DOGGETT NA; FISCHELGHODSIAN N; GARDNER D; GUMUCIO D; KRIZMAN DB; KRUGLYAK L; LEVY E; LIU P; MARRONE BL; PRAS E; PRAS M; RICHARDS RI; ROTTER JI; SHELTON D; SHOHAT M; WOOD G; KASTNER DL
      HIGH-RESOLUTION PHYSICAL MAP OF THE REGION SPANNING THE MEF LOCUS AT 16P13

      Cytogenetics and cell genetics
    74. SHER C; SHARABANIGARGIR L; SHOHAT M
      BREAST-CANCER AND BRCA1 MUTATIONS

      The New England journal of medicine
    75. SHOHAT M; TICK D; BARAKAT S; BU X; MELMED S; RIMOIN DL
      SHORT-TERM RECOMBINANT HUMAN GROWTH-HORMONE TREATMENT INCREASES GROWTH-RATE IN ACHONDROPLASIA

      The Journal of clinical endocrinology and metabolism
    76. JABER L; SHOHAT M; HALPERN GJ
      DEMOGRAPHIC CHARACTERISTICS OF THE ISRAELI ARAB COMMUNITY IN CONNECTION WITH CONSANGUINITY

      Israel journal of medical sciences
    77. MIMOUNI M; MIMOUNIBLOCH A; SCHACHTER J; SHOHAT M
      FAMILIAL HYPOTHYROIDISM WITH AUTOSOMAL-DOMINANT INHERITANCE

      Archives of Disease in Childhood
    78. HALPERN GJ; SHOHAT M; MERLOB P
      PARTIAL TRISOMY 10Q - FURTHER DELINEATION OF THE CLINICAL MANIFESTATIONS INVOLVING THE SEGMENT 10Q23-]10Q24

      Annales de genetique
    79. LEVY EN; SHEN Y; KUPELIAN A; KRUGLYAK L; AKSENTIJEVICH I; PRAS E; BALOW JE; LINZER B; CHEN XG; SHELTON DA; GUMUCIO D; PRAS M; SHOHAT M; ROTTER JI; FISCHELGHODSIAN N; RICHARDS RI; KASTNER DL
      LINKAGE DISEQUILIBRIUM MAPPING PLACES THE GENE CAUSING FAMILIAL MEDITERRANEAN FEVER CLOSE TO D16S246

      American journal of human genetics
    80. IVANOV I; SHUPER A; SHOHAT M; SNIR M; WEITZ R
      ANIRIDIA - RECENT ACHIEVEMENTS IN PEDIATRIC PRACTICE

      European journal of pediatrics
    81. AKSENTIJEVICH I; CHEN X; BALOW JE; LEVY E; PRAS E; GARDNER D; PRAS M; FISCHELGHODSIAN N; KUPELIAN A; SHOHAT M; ROTTER JI; SHEN Y; RICHARDS RI; CALLEN DF; DOGGETT NA; LIU P; BLAKE T; SHELTON D; GUMUCIO D; KASTNER DL
      REFINED LOCALIZATION OF THE GENE CAUSING FAMILIAL MEDITERRANEAN FEVER

      Cytogenetics and cell genetics
    82. SHOHAT M; AKSTEIN E; DAVIDOV B; BARKAI G; LEGUM C; DAVID M; DAR H; ROMEM Y; AMIEL A; COHEN H; BACH G; BENNERIAH Z; SHEFFER RN; APPELMAN Z; CHEMKE J; ZADKA P; ZER T; GOLDMAN B
      AMNIOCENTESIS RATE AND THE DETECTION OF DOWN-SYNDROME AND OTHER CHROMOSOMAL-ANOMALIES IN ISRAEL

      Prenatal diagnosis
    83. BALLIN A; SHOHAT M; MEYTES D
      ACUTE LYMPHOBLASTIC-LEUKEMIA WITH A UNIQUE TRANSLOCATION IN AN ADOLESCENT BOY

      Cancer genetics and cytogenetics
    84. DANIELS M; SHOHAT T; BRENNERULLMAN A; SHOHAT M
      FAMILIAL MEDITERRANEAN-FEVER - HIGH GENE-FREQUENCY AMONG THE NON-ASHKENAZIC AND ASHKENAZIC JEWISH POPULATIONS IN ISRAEL

      American journal of medical genetics
    85. JABER L; WEITZ R; BU XD; FISCHELGHODSIAN N; ROTTER JI; SHOHAT M
      ARTHROGRYPOSIS MULTIPLEX CONGENITA IN AN ARAB KINDRED - UPDATE

      American journal of medical genetics
    86. SHOHAT M; LEGUM C; ROMEM Y; BOROCHOWITZ Z; BACH G; GOLDMAN B
      DOWN-SYNDROME PREVENTION PROGRAM IN A POPULATION WITH AN OLDER MATERNAL AGE

      Obstetrics and gynecology
    87. GORSKY M; SHOHAT M; BUKAI A; MOSKONA D
      THE ROLE OF GENETICS ON THE PREVALENCE OF TORUS PALATINUS

      Journal of dental research
    88. HALPERN GJ; STOUPEL EG; BARKAI G; CHAKI R; LEGUM C; FEJGIN MD; SHOHAT M
      SOLAR-ACTIVITY CYCLE AND THE INCIDENCE OF FETAL CHROMOSOME-ABNORMALITIES DETECTED AT PRENATAL-DIAGNOSIS

      International journal of biometeorology
    89. DRUCE M; COHEN IJ; NAOR N; SHOHAT M
      LATE DIAGNOSIS OF DOWN-SYNDROME DUE TO INCORRECT CYTOGENETIC DIAGNOSIS AND EXTREME PREMATURITY

      Clinical genetics
    90. SHOHAT M; MOR R; SHOHAT T; GADOTH N; ACHIRON A; MAGAL N
      THE HIGHER INCIDENCE OF MYOTONIC-DYSTROPHY (DM) IN NORTH-AFRICAN AND YEMENITE JEWS COMPARED TO ASHKENAZIC JEWS IS ASSOCIATED WITH A SIGNIFICANTLY HIGHER NUMBER OF CTG TRINUCLEOTIDE REPEATS

      American journal of human genetics
    91. AKSENTIJEVICH I; ALTHERR M; APOSTOLOU S; BALOW JE; BLAKE T; CALLEN DF; CENTOLA M; CHEN X; CHEN X; COLLINS FS; DOGGETT NA; FISCHELGHODSIAN N; GARDNER D; GUMUCIO D; KRIZMAN DB; LEVY E; LIU P; MARRONE BL; PRAS E; PRAS M; RICHARDS RI; ROTTER JI; SHELTON D; SHOHAT M; SOOD R; WOOD G; KASTNER DL
      PHYSICAL AND TRANSCRIPTIONAL MAP OF THE FMF CANDIDATE REGION

      American journal of human genetics
    92. JABER L; BAILEYWILSON JE; HAJYEHIA M; HERNANDEZ J; SHOHAT M
      CONSANGUINEOUS MATINGS IN AN ISRAELI-ARAB COMMUNITY

      Archives of pediatrics & adolescent medicine
    93. JABER L; MERLOB P; SHOHAT M
      HIGH-INCIDENCE OF CENTRAL-NERVOUS-SYSTEM MALFORMATIONS ASSOCIATED WITH MARKED PARENTAL CONSANGUINITY IN AN ISRAELI ARAB COMMUNITY

      Biomedicine & pharmacotherapy
    94. APPELMAN Z; MANOR M; MAGAL N; CASPI B; SHOHAT M; BLICKSTEIN I
      PRENATAL-DIAGNOSIS OF TWIN ZYGOSITY BY DNA FINGERPRINT ANALYSIS

      Prenatal diagnosis
    95. STARK B; JEISON M; SHOHAT M; GOSHEN Y; VOGEL R; COHEN IJ; YANIV I; KAPLINSKY C; ZAIZOV R
      INVOLVEMENT OF 11P15 AND 3Q21Q26 IN THERAPY-RELATED MYELOID-LEUKEMIA (T-ML) IN CHILDREN - CASE-REPORTS AND REVIEW OF THE LITERATURE

      Cancer genetics and cytogenetics
    96. BRENNERULLMAN A; MELZEROFIR H; DANIELS M; SHOHAT M
      POSSIBLE PROTECTION AGAINST ASTHMA IN HETEROZYGOTES FOR FAMILIAL MEDITERRANEAN FEVER

      American journal of medical genetics
    97. SHOHAT M; LACHMAN R; GRUBER HE; HSIA YE; GOLBUS MS; WITT DR; BODELL A; BRYKE CR; HOGGE WA; RIMOIN DL
      DESBUQUOIS SYNDROME - CLINICAL, RADIOGRAPHIC, AND MORPHOLOGIC CHARACTERIZATION

      American journal of medical genetics
    98. IKEDA S; WAKEM P; HAAKE A; EWING N; POLAKOWSKA R; SARRET Y; TRATTNER A; DAVID M; SHOHAT M; SCHROEDER DW; EPSTEIN EH; GOLDSMITH LA
      LOCALIZATION OF THE GENE FOR DARIER DISEASE TO A 5-CM INTERVAL ON CHROMOSOME 12Q

      Journal of investigative dermatology
    99. ACHIRON A; MAGAL N; SHEMTOV N; NOY S; SHOHAT M; GADOTH N
      MYOTONIC-DYSTROPHY GENE ANALYSIS IN AFFECTED ISRAELI FAMILIES

      Israel journal of medical sciences
    100. ASH S; JOHNSON C; SHOHAT M; SHOHAT T; SCHLESINGER M
      FURTHER MAPPING OF THE PROPERDIN DEFICIENCY GENE IN A TUNISIAN JEWISHFAMILY - EVIDENCE FOR GENETIC HOMOGENEITY

      Israel journal of medical sciences


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 19:34:39