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La ricerca find articoli where soggetti phrase all words 'ASHKENAZI JEWS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 195 riferimenti
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    1. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    2. Misbahuddin, A; Warner, TT
      Dystonia: an update on genetics and treatment

      CURRENT OPINION IN NEUROLOGY
    3. Bach, G
      Mucolipidosis type IV

      MOLECULAR GENETICS AND METABOLISM
    4. Bergman, A; Einbeigi, Z; Olofsson, U; Taib, Z; Wallgren, A; Karlsson, P; Wahlstrom, J; Martinsson, T; Nordling, M
      The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Olopade, OI; Pichert, G
      Cancer genetics in oncology practice

      ANNALS OF ONCOLOGY
    6. Wunderlich, S; Reiners, K; Gasser, T; Naumann, M
      Cervical dystonia in monozygotic twins: Case report and review of the literature

      MOVEMENT DISORDERS
    7. King, MC; Owens, K
      Genomic views of human history (Reprinted from Science, vol 286, pg 451-453, 1999)

      PATHOLOGIE BIOLOGIE
    8. Major, T; Svetel, M; Romac, S; Kostic, VS
      DYT1 mutation in primary torsion dystonia in a Serbian population

      JOURNAL OF NEUROLOGY
    9. Ghaderi, A; Talei, A; Farjadian, S; Mosalaei, A; Doroudchi, M; Kimura, H
      Germline BRCA1 mutations in Iranian women with breast cancer

      CANCER LETTERS
    10. Arnaiz-Villena, A; Elaiwa, N; Silvera, C; Rostom, A; Moscoso, J; Gomez-Casado, E; Allende, L; Varela, P; Martinez-Laso, J
      The origin of Palestinians and their genetic relatedness with other Mediterranean populations

      HUMAN IMMUNOLOGY
    11. Crawford, MH; Reddy, BM; Martinez-Laso, J; Mack, SJ; Erlich, HA
      Genetic variation among the Golla pastoral caste subdivisions of Andhra Pradesh, India, according to the HLA system

      HUMAN IMMUNOLOGY
    12. Gonzalez, S; Brautbar, C; Martinez-Borra, J; Lopez-Vazquez, A; Segal, R; Blanco-Gelaz, MA; Enk, CD; Safriman, C; Lopez-Larrea, C
      Polymorphism in MICA rather than HLA-B/C genes is associated with psoriatic arthritis in the Jewish population

      HUMAN IMMUNOLOGY
    13. Klitz, W; Brautbar, C; Schito, AM; Barcellos, LF; Oksenberg, JR
      Evolution of the CCR5 Delta 32 mutation based on haplotype variation in Jewish and northern European population samples

      HUMAN IMMUNOLOGY
    14. Kwon, OJ; Brautbar, C; Weintrob, N; Sprecher, E; Saphirman, C; Bloch, K; Pinhas-Hamiel, O; Assah, S; Vardi, P; Israel, S
      Immunogenetics of HLA class II in Israeli Ashkenazi Jewish, Israeli non-Ashkenazi Jewish, and in Israeli Arab IDDM patients

      HUMAN IMMUNOLOGY
    15. Bach, G; Tomczak, J; Risch, N; Ekstein, J
      Tay-sachs screening in the Jewish Ashkenazi population: DNA testing is thepreferred procedure

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Schwartz, MD; Rothenberg, K; Joseph, L; Benkendorf, J; Lerman, C
      Consent to the use of stored DNA for genetics research: A survey of attitudes in the Jewish population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Subramanian, G; Adams, MD; Venter, JC; Broder, S
      Implications of the human genome for understanding human biology and medicine

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    18. Suzuki, K
      Recognition and delineation of beta-hexosaminidase alpha-chain variants: Ahistorical and personal perspective

      TAY-SACHS DISEASE
    19. Risch, N
      Molecular epidemiology of Tay-Sachs disease

      TAY-SACHS DISEASE
    20. Matsubara, A; Wasson, JC; Donelan, SS; Welling, CM; Glaser, B; Permutt, MA
      Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes

      DIABETOLOGIA
    21. Permutt, MA; Wasson, JC; Suarez, BK; Lin, J; Thomas, J; Meyer, J; Lewitzky, S; Rennich, JS; Parker, A; DuPrat, L; Maruti, S; Chayen, S; Glaser, B
      A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population

      DIABETES
    22. Dossenbach-Glaninger, A; Krugluger, W; Schrattbauer, K; Eder, S; Hopmeier, P
      Severe factor XI deficiency caused by compound heterozygosity for the typeIII mutation and a novel insertion in exon 9 (codons 324/325+G)

      BRITISH JOURNAL OF HAEMATOLOGY
    23. Figer, A; Shtoyerman-Chen, R; Tamir, A; Geva, R; Irmin, L; Flex, D; Theodor, L; Sulkes, A; Sadetzki, S; Bar-Meir, S; Friedman, E
      Phenotypic characteristics of colo-rectal cancer in I1307K APC germline mutation carriers compared with sporadic cases

      BRITISH JOURNAL OF CANCER
    24. Figer, A; Irmin, L; Geva, R; Flex, D; Sulkes, A; Friedman, E
      Genetic analysis of the APC gene regions involved in attenuated APC phenotype in Israeli patients with early onset and familial colorectal cancer

      BRITISH JOURNAL OF CANCER
    25. Chen-Shtoyerman, R; Figer, A; Fidder, HH; Rath, P; Yeremin, L; Bar Meir, S; Friedman, E; Theodor, L
      The frequency of the predominant Jewish mutations in BRCA1 and BRCA2 in unselected Ashkenazi colorectal cancer patients

      BRITISH JOURNAL OF CANCER
    26. Figer, A; Irmin, L; Geva, R; Flex, D; Sulkes, J; Sulkes, A; Friedman, E
      The rate of the 6174delT founder Jewish mutation in BRCA2 in patients withnon-colonic gastrointestinal tract tumours in Israel

      BRITISH JOURNAL OF CANCER
    27. Arnaiz-Villena, A; Karin, M; Bendikuze, N; Gomez-Casado, E; Moscoso, J; Silvera, C; Oguz, FS; Diler, AS; de Pacho, A; Allende, L; Guillen, J; Laso, JM
      HLA alleles and haplotypes in the Turkish population: relatedness to Kurds, Armenians and other Mediterraneans

      TISSUE ANTIGENS
    28. Arnaiz-Villena, A; Dimitroski, K; Pacho, A; Moscoso, J; Gomez-Casado, E; Silvera-Redondo, C; Varela, P; Blagoevska, M; Zdravkovska, V; Martinez-Laso, J
      HLA genes in Macedonians and the sub-Saharan origin of the Greeks

      TISSUE ANTIGENS
    29. Mazarib, A; Simon, ES; Korczyn, AD; Falik-Zaccai, Z; Gazit, E; Giladi, N
      Hereditary juvenile-onset craniocervical predominant generalized dystonia with parkinsonism

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    30. Slatkin, M; Rannala, B
      Estimating allele age

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    31. Yair, D; Ben Baruch, G; Chetrit, A; Friedman, T; Yechezkel, GH; Gotlieb, WH; Fishman, A; Beller, U; Bar-Am, A; Friedman, E
      p53 and WAF1 polymorphisms in Jewish-Israeli women with epithelial ovariancancer and its association with BRCA mutations

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    32. Bolton-Maggs, PHB
      Factor XI deficiency and its management

      HAEMOPHILIA
    33. Tian, HJ; Brody, LC; Landers, JP
      Rapid detection of deletion, insertion, and substitution mutations via heteroduplex analysis using capillary- and microchip-based electrophoresis

      GENOME RESEARCH
    34. Bouma, BN; Meijers, JCM
      Role of blood coagulation factor XI in downregulation of fibrinolysis

      CURRENT OPINION IN HEMATOLOGY
    35. Grzybowska, E; Zientek, H; Jasinska, A; Rusin, M; Kozlowski, P; Sobczak, K; Sikorska, A; Kwiatkowska, E; Gorniak , L; Kalinowska, E; Utracka-Hutka, B; Wloch, J; Chmielik, E; Krzyzosiak, WJ
      High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer

      HUMAN MUTATION
    36. Shiri-Sverdlov, R; Oefner, P; Green, L; Baruch, RG; Wagner, T; Kruglikova, A; Haitchick, S; Hofstra, RMW; Papa, MZ; Mulder, I; Rizel, S; Sade, RBB; Dagan, E; Abdeen, Z; Goldman, B; Friedman, E
      Mutational analyses of BRCA1 and BRCA2 with Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

      HUMAN MUTATION
    37. Liu, MC; Drury, KC; Kipersztok, S; Zheng, WR; Williams, RS
      Primer system for single cell detection of double mutation for Tay-Sachs disease

      JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
    38. Cui, JS; Hopper, JL
      Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    39. Korf, BR
      Integration of genetics into medical practice: ethical, legal, and social perspective

      CURRENT OPINION IN PEDIATRICS
    40. Hewett, J; Gonzalez-Agosti, C; Slater, D; Ziefer, P; Li, S; Bergeron, D; Jacoby, DJ; Ozelius, LJ; Ramesh, V; Breakefield, XO
      Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

      HUMAN MOLECULAR GENETICS
    41. Kawaguchi, T; Koga, S; Hongo, H; Komiyama, Y; Li, K; Ishihara, S; Horikawa, K; Hidaka, M; Mitsuya, H; Nakakuma, H
      A novel type of factor XI deficiency showing compound genetic abnormalities: A nonsense mutation and an impaired transcription

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    42. Hamann, HA; Croyle, RT; Smith, KR; Quan, BNM; McCance, KL; Botkin, JR
      Interest in a support group among individuals tested for a BRCA1 gene mutation

      JOURNAL OF PSYCHOSOCIAL ONCOLOGY
    43. Levy-Lahad, E; Krieger, M; Gottfeld, O; Renbaum, P; Klein, G; Eisenberg, S; Lahad, A; Kaufman, B; Catane, R
      BRCA1 and BRCA2 mutation carriers as potential candidates for chemoprevention trials

      JOURNAL OF CELLULAR BIOCHEMISTRY
    44. Nomura, Y; Ikeuchi, T; Tsuji, S; Segawa, M
      Two phenotypes and anticipation observed in Japanese cases with early onset torsion dystonia (DYT1) - pathophysiological consideration

      BRAIN & DEVELOPMENT
    45. Sato, E; Kawamata, N; Kato, A; Oshimi, K
      A novel mutation that leads to a congenital factor XI deficiency in a Japanese family

      AMERICAN JOURNAL OF HEMATOLOGY
    46. Colombo, R; Bignamini, AA; Carobene, A; Sasaki, J; Tachikawa, M; Kobayashi, K; Toda, T
      Age and origin of the FCMD 3 '-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population

      HUMAN GENETICS
    47. Ventura, C; Santos, AIM; Tavares, A; Gago, T; Lavinha, J; McVey, JH; David, D
      Molecular genetic analysis of factor XI deficiency: Identification of fivenovel gene alterations and the origin of type II mutation in Portuguese families

      THROMBOSIS AND HAEMOSTASIS
    48. Drucker, L; Stackievitz, R; Shpitz, B; Yarkoni, S
      Incidence of BRCA1 and BRCA2 mutations in Ashkenazi colorectal cancer patients: Preliminary study

      ANTICANCER RESEARCH
    49. Hamann, HA; Croyle, RT; Venne, VL; Baty, BJ; Smith, KR; Botkin, JR
      Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Johnson, KA; Rosenblum-Vos, L; Petersen, GM; Brensinger, JD; Giardiello, FM; Griffin, CA
      Response to genetic counseling and testing for the APC I1307K mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Glaser, B
      Hyperinsulinism of the newborn

      SEMINARS IN PERINATOLOGY
    52. Fishman, A; Dekel, E; Chetrit, A; Lerner-Geva, L; Bar-Am, A; Beck, D; Beller, U; Ben-Baruch, G; Piura, B; Friedman, E; Struewing, JP; Modan, B
      Patients with double primary tumors in the breast and ovary - Clinical characteristics and BRCA1-2 mutations status

      GYNECOLOGIC ONCOLOGY
    53. Illarioshkin, SN; Markova, ED; Miklina, NI; Ivanova-Smolenskaya, IA
      Molecular genetics of the hereditary dystonic syndromes

      ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA
    54. Gibbs, SR; Blitzer, A
      Botulinum toxin for the treatment of spasmodic dysphonia

      OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
    55. Meijers, JCM; Tekelenburg, WLH; Bouma, BN; Bertina, RM; Rosendaal, FR
      High levels of coagulation factor XI as a risk factor for venous thrombosis.

      NEW ENGLAND JOURNAL OF MEDICINE
    56. Bressman, SB; Sabatti, C; Raymond, D; de Leon, D; Klein, C; Kramer, PL; Brin, MF; Fahn, S; Breakefield, X; Ozelius, LJ; Risch, NJ
      The DYT1 phenotype and guidelines for diagnostic testing

      NEUROLOGY
    57. Klein, C; Kann, M; Kis, B; Pramstaller, PP; Breakefield, XO; Ozelius, LJ; Vieregge, P
      The genetics of dystonia

      NERVENARZT
    58. Diez, O; Campos, B; Baiget, M
      Molecular diagnosis for hereditary cancer

      MEDICINA CLINICA
    59. Kustedjo, K; Bracey, MH; Cravatt, BF
      Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations

      JOURNAL OF BIOLOGICAL CHEMISTRY
    60. Drucker, L; Shpilberg, O; Neumann, A; Shapira, J; Stackievicz, R; Beyth, Y; Yarkoni, S
      Adenomatous polyposis coli I1307K mutation in Jewish patients with different ethnicity - Prevalence and phenotype

      CANCER
    61. Shirk, RA; Konkle, BA; Walsh, PN
      Nonsense mutation in exon V of the factor XI gene does not abolish platelet factor XI expression

      BRITISH JOURNAL OF HAEMATOLOGY
    62. Tamary, H; Bar-Yam, R; Shalmon, L; Rachavi, G; Krostichevsky, M; Elhasid, R; Barak, Y; Kapelushnik, J; Yaniv, I; Auerbach, AD; Zaizov, R
      Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients

      BRITISH JOURNAL OF HAEMATOLOGY
    63. Papelard, H; de Bock, GH; van Eijk, R; Vlieland, TPMV; Cornelisse, CJ; Devilee, P; Tollenaar, RAEM
      Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patients

      BRITISH JOURNAL OF CANCER
    64. Gershoni-Baruch, R; Patael, Y; Dagan; Figer, A; Kasinetz, L; Kadouri, E; Bar Sade, RB; Friedman, E
      Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers

      BRITISH JOURNAL OF CANCER
    65. Shashidharan, P; Kramer, BC; Walker, RH; Olanow, CW; Brin, MF
      Immunohistochemical localization and distribution of torsinA in normal human and rat brain

      BRAIN RESEARCH
    66. Brassat, D; Camuzat, A; Vidailhet, M; Feki, I; Jedynak, P; Klap, P; Agid, Y; Durr, A; Brice, A
      Frequency of the DYT1 mutation in primary torsion dystonia without family history

      ARCHIVES OF NEUROLOGY
    67. Glaser, B; Thornton, P; Otonkoski, T; Junien, C
      Genetics of neonatal hyperinsulinism

      ARCHIVES OF DISEASE IN CHILDHOOD
    68. Diaz, A; Montfort, M; Cormand, B; Zeng, BJ; Pastores, GM; Chabas, A; Vilageliu, L; Grinberg, D
      On the age of the most prevalent Gaucher disease-causing mutation, N370S

      AMERICAN JOURNAL OF HUMAN GENETICS
    69. Gomez-Casado, E; del Moral, P; Martinez-Laso, J; Garcia-Gomez, A; Allende, L; Silvera-Redondo, C; Longas, J; Gonzalez-Hevilla, M; Kandil, M; Zamora, J; Arnaiz-Villena, A
      HLA genes in Arabic-speaking Moroccans: close relatedness to Berbers and Iberians

      TISSUE ANTIGENS
    70. Tanaka, A; Fujimaru, M; Choeh, K; Isshiki, G
      Novel mutations including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patientswith Tay-Sachs disease

      JOURNAL OF HUMAN GENETICS
    71. Bauduer, F; Dupreuilh, F; Ducout, L; Marti, B
      Factor XI deficiency in the French Basque Country

      HAEMOPHILIA
    72. Glaser, B; Furth, J; Stanley, CA; Baker, L; Thornton, PS; Landau, H; Permutt, MA
      Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism

      HUMAN MUTATION
    73. Patael, Y; Figer, A; Gershoni-Baruch, R; Papa, MZ; Risel, S; Shtoyerman-Chen, R; Karasik, A; Theodor, L; Friedman, E
      Common origin of the I1307K APC polymorphism in Ashkenazi and non-Ashkenazi Jews

      EUROPEAN JOURNAL OF HUMAN GENETICS
    74. Raas-Rothschild, A; Bargal, R; DellaPergola, S; Zeigler, M; Bach, G
      Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    75. Thyagarajan, D
      Dystonia: recent advances

      JOURNAL OF CLINICAL NEUROSCIENCE
    76. Yin, J; Harpaz, N; Souza, RF; Zou, TT; Kong, DH; Wang, SN; Leytin, AL; Medalie, NS; Smolinski, KN; Abraham, JM; Fleisher, AS; Meltzer, SJ
      Low prevalence of the APC I1307K sequence in Jewish and non-Jewish patients with inflammatory bowel disease

      ONCOGENE
    77. Thomas, PM
      Genetic mutations as a cause of hyperinsulinemic hypoglycemia in children

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    78. Ozelius, LJ; Page, CE; Klein, C; Hewett, JW; Mineta, M; Leung, J; Shalish, C; Bressman, SB; de Leon, D; Brin, MF; Fahn, S; Corey, DP; Breakefield, XO
      The TOR1A (DYT1) gene family and its role in early onset torsion dystonia

      GENOMICS
    79. Kamm, C; Castelon-Konkiewitz, E; Naumann, M; Heinen, F; Brack, M; Nebe, A; Ceballos-Baumann, A; Gasser, T
      GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany

      MOVEMENT DISORDERS
    80. Kadir, RA; Economides, DL; Lee, CA
      Factor XI deficiency in women

      AMERICAN JOURNAL OF HEMATOLOGY
    81. Klein, C; Breakefield, XO; Ozelius, LJ
      Genetics of primary dystonia

      SEMINARS IN NEUROLOGY
    82. Rady, PL; Tyring, SK; Hudnall, SD; Vargas, T; Kellner, LH; Nitowsky, H; Matalon, RK
      Methylenetetrahydrofolate reductase (MTHFR): The incidence of mutations C677T and A1298C in the Ashkenazi Jewish population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    83. Shaag, A; Saada, A; Berger, I; Mandel, H; Joseph, A; Feigenbaum, A; Elpeleg, ON
      Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Hornreich, G; Beller, U; Lavie, O; Renbaum, P; Cohen, Y; Levy-Lahad, E
      Is uterine serous papillary carcinoma a BRCA1-related disease? Case reportand review of the literature

      GYNECOLOGIC ONCOLOGY
    85. Kadir, RA
      Women and inherited bleeding disorders: Pregnancy and delivery

      SEMINARS IN HEMATOLOGY
    86. Owens, K; King, MC
      Genomic views of human history

      SCIENCE
    87. Limborska, SA
      Human molecular genetics: Medical-genetic and population studies

      MOLECULAR BIOLOGY
    88. Lynch, HT; de la Chapelle, A
      Genetic susceptibility to non-polyposis colorectal cancer

      JOURNAL OF MEDICAL GENETICS
    89. Holtzman, NA
      Promoting safe and effective genetic tests in the United States: Work of the Task Force on Genetic Testing

      CLINICAL CHEMISTRY
    90. Alhaq, A; Mitchell, M; Sethi, M; Rahman, S; Flynn, G; Boulton, P; Caeno, G; Smith, M; Savidge, G
      Identification of a novel mutation in a non-Jewish factor XI deficient kindred

      BRITISH JOURNAL OF HAEMATOLOGY
    91. Lebre, AS; Durr, A; Jedynak, P; Ponsot, G; Vidailhet, M; Agid, Y; Brice, A
      DYT1 mutation in French families with idiopathic torsion dystonia

      BRAIN
    92. Martincic, D; Kravtsov, V; Gailani, D
      Factor XI messenger RNA in human platelets

      BLOOD
    93. Dorum, A; Heimdal, K; Hovig, E; Inganas, M; Moller, P
      Penetrances of BRCA1 1675delA and 1135insA with respect to breast cancer and ovarian cancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    94. Blumenfeld, A; Slaugenhaupt, SA; Liebert, CB; Temper, V; Maayan, C; Gill, S; Lucente, DE; Idelson, M; MacCormack, K; Monahan, MA; Mull, J; Leyne, M; Mendillo, M; Schiripo, T; Mishori, E; Breakefield, X; Axelrod, FB; Gusella, JF
      Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31

      AMERICAN JOURNAL OF HUMAN GENETICS
    95. Maresco, DL; Arnold, PH; Sonoda, Y; Federici, MG; Bogomolniy, F; Rhei, E; Boyd, J
      The APC I1307K allele and BRCA-associated ovarian cancer risk

      AMERICAN JOURNAL OF HUMAN GENETICS
    96. Terdiman, JP; Conrad, PG; Sleisenger, MH
      Genetic testing in hereditary colorectal cancer: Indications and procedures

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    97. Leube, B; Kessler, KR; Ferbert, A; Ebke, M; Schwendemann, G; Erbguth, F; Benecke, R; Auburger, G
      Phenotypic variability of the DYT1 mutation in German dystonia patients

      ACTA NEUROLOGICA SCANDINAVICA
    98. Arnaiz-Villena, A; Iliakis, P; Gonzalez-Hevilla, M; Longas, J; Gomez-Casado, E; Sfyridaki, K; Trapaga, J; Silvera-Redondo, C; Matsouka, C; Martinez-Laso, J
      The origin of Cretan populations as determined by characterization of HLA alleles

      TISSUE ANTIGENS
    99. Tang, NLS; Pang, CP; Yeo, W; Choy, KW; Lam, PK; Suen, M; Law, LK; King, WWK; Johnson, P; Hjelm, M
      Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    100. YAKOBSON EA; ZLOTOGORSKI A; SHAFIR R; COHEN M; ICEKSON M; LANDAU M; BRENNER S; USHER S; PERETZ H
      SCREENING FOR TUMOR-SUPPRESSOR P16(CDKN2A) GERMLINE MUTATIONS IN ISRAELI MELANOMA FAMILIES

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 16:15:18