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    1. Yang, HY; Ohmen, JD; Ma, YH; Targan, SR; FischelGhodsian, N; Rotter, JI
      Additional evidence of linkage between Crohn's disease and a putative locus on chromosome 12 (vol 1, pg 194, 1999)

      GENETICS IN MEDICINE
    2. FISCHELGHODSIAN N
      MITOCHONDRIAL RNA PROCESSING AND TRANSLATION - LINK BETWEEN MITOCHONDRIAL MUTATIONS AND HEARING-LOSS

      Molecular genetics and metabolism ( Molecular genetics and metabolism (Print))
    3. 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
    4. DENG ZM; CENTOLA M; CHEN XG; SOOD R; VEDULA A; FISCHELGHODSIAN N; KASTNER DL
      IDENTIFICATION OF 2 KRUPPEL-RELATED ZINC-FINGER GENES (ZNF200 AND ZNF210) FROM HUMAN-CHROMOSOME 16P13.3

      Genomics (San Diego, Calif.)
    5. JOHNSON DF; HAMON M; FISCHELGHODSIAN N
      CHARACTERIZATION OF THE HUMAN MITOCHONDRIAL RIBOSOMAL S12 GENE

      Genomics (San Diego, Calif.)
    6. JOHNSON DF; PREZANT TR; LUBAVIN B; CHALTRAW WE; FISCHELGHODSIAN N
      ISOLATION OF OVEREXPRESSED YEAST GENES WHICH PREVENT AMINOGLYCOSIDE TOXICITY

      Hearing research
    7. GUAN MX; ENRIQUEZ JA; FISCHELGHODSIAN N; PURANAM RS; LIN CP; MAW MA; ATTARDI G
      THE DEAFNESS-ASSOCIATED MITOCHONDRIAL-DNA MUTATION AT POSITION-7445, WHICH AFFECTS TRNA(SER(UCN)) PRECURSOR PROCESSING, HAS LONG-RANGE EFFECTS ON NADH DEHYDROGENASE SUBUNIT ND6 GENE-EXPRESSION

      Molecular and cellular biology
    8. CASANO RAMS; BYKHOVSKAYA Y; JOHNSON DF; HAMON M; TORRICELLI F; BIGOZZI M; FISCHELGHODSIAN N
      HEARING-LOSS DUE TO THE MITOCHONDRIAL A1555G MUTATION IN ITALIAN FAMILIES

      American journal of medical genetics
    9. 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
    10. SEVIOR KB; HATAMOCHI A; STEWART IA; BYKHOVSKAYA Y; ALLENPOWELL DR; FISCHELGHODSIAN N; MAW MA
      MITOCHONDRIAL A7445G MUTATION IN 2 PEDIGREES WITH PALMOPLANTAR KERATODERMA AND DEAFNESS

      American journal of medical genetics
    11. FISCHELGHODSIAN N
      MITOCHONDRIAL GENETICS AND HEARING-LOSS - THE MISSING LINK BETWEEN GENOTYPE AND PHENOTYPE

      Proceedings of the Society for Experimental Biology and Medicine
    12. TAYLOR KD; LI Z; BARRY M; FISCHELGHODSIAN N; PLEVY SE; ROTTER JI; TARGAN SR; YANG H
      TUMOR-NECROSIS-FACTOR MICROSATELLITE HAPLOTYPE A11B4C1D3E3 IS ASSOCIATED WITH ANTI-SACCAROMYCES CERVISIAE ANTIBODY (ASCA) ACROSS CLINICAL FORMS OF INFLAMMATORY BOWEL-DISEASE

      Gastroenterology
    13. YANG H; OHMEN JD; MA R; LI Z; BENTLEY LG; TARGAN SR; FISCHELGHODSIAN N; ROTTER JI
      LINKAGE AND ASSOCIATION BETWEEN CROHNS-DISEASE AND A PUTATIVE LOCUS ON CHROMOSOME-12

      Gastroenterology
    14. LINKERISRAELI M; WALLACE DJ; MICHAEL D; PREHN J; NAND R; TAYLOR KD; PAULLABRADOR M; HONDA M; FISCHELGHODSIAN N; FRASER PA; KLINENBERG JR
      NOVEL ALLELES OF THE IL-6 GENE MINISATELLITE ARE ASSOCIATED WITH SYSTEMIC LUPUS-ERYTHEMATOSUS (SLE) AND WITH DIFFERENTIAL IL-6 EXPRESSION

      Arthritis and rheumatism
    15. FISCHELGHODSIAN N
      MITOCHONDRIAL MUTATIONS AND HEARING-LOSS - PARADIGM FOR MITOCHONDRIALGENETICS

      American journal of human genetics
    16. HYSLOP SJ; JAMES AM; MAW M; FISCHELGHODSIAN N; MURPHY MP
      THE EFFECT ON MITOCHONDRIAL-FUNCTION OF THE TRNA(SER(UCN)) COI A7445GMTDNA POINT MUTATION ASSOCIATED WITH MATERNALLY-INHERITED SENSORINEURAL DEAFNESS/

      Biochemistry and molecular biology international
    17. 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
    18. 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
    19. FISCHELGHODSIAN N; BYKHOVSKAYA Y; TAYLOR K; KAHEN T; CANTOR R; EHRENMAN K; SMITH R; KEITHLEY E
      TEMPORAL BONE ANALYSIS OF PATIENTS WITH PRESBYCUSIS REVEALS HIGH-FREQUENCY OF MITOCHONDRIAL MUTATIONS

      Hearing research
    20. FISCHELGHODSIAN N; PREZANT TR; CHALTRAW WE; WENDT KA; NELSON RA; ARNOS KS; FALK RE
      MITOCHONDRIAL GENE MUTATION IS A SIGNIFICANT PREDISPOSING FACTOR IN AMINOGLYCOSIDE OTOTOXICITY

      American journal of otolaryngology
    21. 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
    22. PANDYA A; XIA X; RADNAABAZAR J; BATSUURI J; DANGAANSUREN B; FISCHELGHODSIAN N; NANCE WE
      MUTATION IN THE MITOCHONDRIAL 12S RIBOSOMAL-RNA GENE IN 2 FAMILIES FROM MONGOLIA WITH MATRILINEAL AMINOGLYCOSIDE OTOTOXICITY

      Journal of Medical Genetics
    23. FRIEDMAN RA; BYKHOVSKAYA Y; TU G; TALBOT JM; WILSON DF; PARNES LS; FISCHELGHODSIAN N
      MOLECULAR ANALYSIS OF THE POU3F4 GENE IN PATIENTS WITH CLINICAL AND RADIOGRAPHIC EVIDENCE OF X-LINKED MIXED DEAFNESS WITH PERILYMPHATIC GUSHER

      The Annals of otology, rhinology & laryngology
    24. 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
    25. 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
    26. 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
    27. 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
    28. 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
    29. JOHNSON DF; PREZANT TR; LUBAVIN B; CHALTRAW WE; FISCHELGHODSIAN N
      IDENTIFICATION OF OVEREXPRESSED YEAST GENES THAT CONFER NEOMYCIN RESISTANCE

      American journal of human genetics
    30. GUAN MX; ENRIQUEZ JA; FISCHELGHODSIAN N; ATTARDI G
      PATHOGENETIC MECHANISM OF THE MITOCHONDRIAL TRNASER(UCN) PRECURSOR-7445 MUTATION AND COEXISTING COMPLEX-I SUBUNIT MTDNA MUTATIONS ASSOCIATED WITH NON-SYNDROMIC DEAFNESS

      American journal of human genetics
    31. CHEN X; HAMON M; CENTOLA M; ROTTER JI; FISCHELGHODSIAN N
      EXCLUSION OF FMFC7, A PUTATIVE C2H2 TYPE ZINC-FINGER PROTEIN AS A CANDIDATE GENE FOR FAMILIAL MEDITERRANEAN FEVER (FMF)

      American journal of human genetics
    32. 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
    33. PREZANT TR; CHALTRAW WE; FISCHELGHODSIAN N
      IDENTIFICATION OF AN OVEREXPRESSED YEAST GENE WHICH PREVENTS AMINOGLYCOSIDE TOXICITY

      Microbiology
    34. SCHEUNER MT; TAYLOR KD; CANTOR RM; FISCHELGHODSIAN N; KHAN SS; FORRESTER JS; ROTTER JI
      A SEARCH FOR GENETIC-DETERMINANTS OF THE RATE OF PROGRESSION TO CORONARY-ARTERY BYPASS GRAFT-SURGERY - THE LIPOPROTEIN-LIPASE LOCUS

      Journal of investigative medicine
    35. DEKOK YJM; VOSSENAAR ER; CREMERS CWRJ; DAHL N; LAPORTE J; HU LJ; LACOMBE D; FISCHELGHODSIAN N; FRIEDMAN RA; PARNES LS; THORPE P; BITNERGLINDZICZ M; PANDER HJ; HEILBRONNER H; GRAVELINE J; DENDUNNEN JT; BRUNNER HG; ROPERS HH; CREMERS FPM
      IDENTIFICATION OF A HOT-SPOT FOR MICRODELETIONS IN PATIENTS WITH X-LINKED DEAFNESS TYPE-3 (DFN3) 900 KB PROXIMAL TO THE DFN3 GENE POU3F4

      Human molecular genetics
    36. GUAN MX; FISCHELGHODSIAN N; ATTARDI G
      BIOCHEMICAL-EVIDENCE FOR NUCLEAR GENE INVOLVEMENT PHENOTYPE OF NON-SYNDROMIC DEAFNESS ASSOCIATED WITH MITOCHONDRIAL 12S RIBOSOMAL-RNA MUTATION

      Human molecular genetics
    37. OHMEN JD; YANG HY; YAMAMOTO KK; ZHAO HY; MA YH; BENTLEY LG; HUANG ZH; GERWEHR S; PRESSMAN S; MCELREE C; TARGAN S; ROTTER JI; FISCHELGHODSIAN N
      SUSCEPTIBILITY LOCUS FOR INFLAMMATORY BOWEL-DISEASE ON CHROMOSOME-16 HAS A ROLE IN CROHNS-DISEASE, BUT NOT IN ULCERATIVE-COLITIS

      Human molecular genetics
    38. 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
    39. MACHE CJ; GORIUP U; FISCHELGHODSIAN N; CHEN X; SCHWINGSHANDL J
      AUTOSOMAL-DOMINANT FAMILIAL MEDITERRANEAN FEVER - LIKE SYNDROME

      European journal of pediatrics
    40. 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
    41. 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
    42. BACINO C; PREZANT TR; BU XD; FOURNIER P; FISCHELGHODSIAN N
      SUSCEPTIBILITY MUTATIONS IN THE MITOCHONDRIAL SMALL RIBOSOMAL-RNA GENE IN AMINOGLYCOSIDE INDUCED DEAFNESS

      Pharmacogenetics
    43. 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
    44. FISCHELGHODSIAN N; PREZANT TR; FOURNIER P; STEWART IA; MAW M
      MITOCHONDRIAL MUTATION ASSOCIATED WITH NONSYNDROMIC DEAFNESS

      American journal of otolaryngology
    45. BHATT S; SCHRECK R; GRAHAM JM; KORENBERG JR; HURVITZ CG; FISCHELGHODSIAN N
      TRANSIENT LEUKEMIA WITH TRISOMY-21 - DESCRIPTION OF A CASE AND REVIEWOF THE LITERATURE

      American journal of medical genetics
    46. BACINO CA; SCHRECK R; FISCHELGHODSIAN N; PEPKOWITZ S; PREZANT TR; GRAHAM JM
      CLINICAL AND MOLECULAR STUDIES IN FULL TRISOMY-22 - FURTHER DELINEATION OF THE PHENOTYPE AND REVIEW OF THE LITERATURE

      American journal of medical genetics
    47. SEPEHRNIA B; PREZANT TR; ROTTER JI; PETTITT DJ; KNOWLER WC; FISCHELGHODSIAN N
      SCREENING FOR MTDNA DIABETES MUTATIONS IN PIMA-INDIANS WITH NIDDM

      American journal of medical genetics
    48. 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
    49. PREZANT TR; CHALTRAW WE; FISCHELGHODSIAN N
      AMINOGLYCOSIDE TOXICITY - THE ISOLATION OF A YEAST GENE INVOLVED IN AMINOGLYCOSIDE RESISTANCE

      American journal of human genetics
    50. 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
    51. PREZANT TR; AGAPIAN JV; FISCHELGHODSIAN N
      CORRECTIONS TO THE HUMAN MITOCHONDRIAL RIBOSOMAL-RNA SEQUENCES

      Human genetics
    52. GARBER A; CARLSON D; SCHRECK R; FISCHELGHODSIAN N; HSU WT; OEZTAS S; PEPKOWITZ S; GRAHAM JM
      PRENATAL-DIAGNOSIS AND DYSMORPHIC FINDINGS IN MOSAIC TRISOMY-16

      Prenatal diagnosis
    53. PREZANT TR; AGAPIAN JV; BOHLMAN MC; BU XD; OZTAS S; QIU WQ; ARNOS KS; CORTOPASSI GA; JABER L; ROTTER JI; SHOHAT M; FISCHELGHODSIAN N
      MITOCHONDRIAL RIBOSOMAL-RNA MUTATION ASSOCIATED WITH BOTH ANTIBIOTIC-INDUCED AND NON-SYNDROMIC DEAFNESS

      Nature genetics
    54. FISCHELGHODSIAN N; PREZANT TR; BU XD; OZTAS S
      MITOCHONDRIAL RIBOSOMAL-RNA GENE MUTATION IN A PATIENT WITH SPORADIC AMINOGLYCOSIDE OTOTOXICITY

      American journal of otolaryngology
    55. FISCHELGHODSIAN N; BU XD; PREZANT TR; OEZTAS S; HUANG ZS; BOHLMAN MC; ROTTER JI; SHOHAT M
      REGIONAL MAPPING OF THE GENE FOR FAMILIAL MEDITERRANEAN FEVER ON HUMAN-CHROMOSOME 16P13

      American journal of medical genetics
    56. BERNES SM; BACINO C; PREZANT TR; PEARSON MA; WOOD TS; FOURNIER P; FISCHELGHODSIAN N
      IDENTICAL MITOCHONDRIAL-DNA DELETION IN MOTHER WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND SON WITH PEARSON MARROW-PANCREAS SYNDROME

      The Journal of pediatrics
    57. UMIEL T; TARYLEHMANN M; RAYNER S; FORSTHUBER T; LEHMANN PV; UITTENBOGAART C; FISCHELGHODSIAN N
      T-CELL SPECIFIC ANTIBODIES AS TREATMENT FOR HUMAN LEUKEMIA IN SCID MICE

      Blood
    58. HUTCHIN TP; STONEKING M; QIU WQ; FISCHELGHODSIAN N; CORTOPASSI G
      ASSOCIATION OF A PARTICULAR POINT MUTATION OF THE MITOCHONDRIAL-DNA WITH AMINOGLYCOSIDE-INDUCED DEAFNESS

      American journal of human genetics
    59. FISCHELGHODSIAN N; PREZANT TR; BU X; BACINO C; OZTAS S
      MITOCHONDRIAL RIBOSOMAL-RNA ANALYSIS IN PATIENTS WITH SPORADIC AMINOGLYCOSIDE OTOTOXICITY

      American journal of human genetics
    60. BACINO CA; GRAHAM JM; FISCHELGHODSIAN N; HSU WT; SCHRECK R
      NON-MOSAIC TRISOMY-22 - A LETHAL TRISOMY SURVIVING TO LATE-GESTATION

      American journal of human genetics
    61. HSU WT; GARBER A; CARLSON D; FISCHELGHODSIAN N; GRAHAM JM; LINN S; WHEELER M; OZTAS S; SCHRECK R
      PRENATAL DETECTED TRISOMY-16 IN 2 PHENOTYPICALLY ABNORMAL NEWBORNS

      American journal of human genetics


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Documento generato il 27/10/20 alle ore 14:15:08