188 related articles for article (PubMed ID: 17149387)
21. Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community.
Jaber L; Merlob P; Bu X; Rotter JI; Shohat M
Am J Med Genet; 1992 Sep; 44(1):1-6. PubMed ID: 1519638
[TBL] [Abstract][Full Text] [Related]
22. The frequency of consanguineous marriage in eastern Turkey.
Akbayram S; Sari N; Akgün C; Doğan M; Tuncer O; Caksen H; Oner AF
Genet Couns; 2009; 20(3):207-14. PubMed ID: 19852426
[TBL] [Abstract][Full Text] [Related]
23. [A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].
Zhou YQ; Mo QH; Lu JH; Li LY; Liang X; Jia SQ; Xiao GF; Zhou WJ; Xiao QZ; Xu XM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun; 25(3):256-61. PubMed ID: 18543211
[TBL] [Abstract][Full Text] [Related]
24. Attitudes of couples identified through screening as carriers of Gaucher disease type 1.
Zuckerman S; Lahad A; Zimran A; Levy-Lahad E; Sagi M
Clin Genet; 2008 Dec; 74(6):566-70. PubMed ID: 18651845
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of beta-thalassemia in Southern Punjab, Pakistan.
Baig SM; Azhar A; Hassan H; Baig JM; Aslam M; Ud Din MA; Qureshi JA; Zaman T
Prenat Diagn; 2006 Oct; 26(10):903-5. PubMed ID: 16821247
[TBL] [Abstract][Full Text] [Related]
26. [Diagnosis and genetic counseling in mental retardation].
Lao Villadóniga JI
Rev Neurol; 2001 Oct; 33 Suppl 1():S1-6. PubMed ID: 12447810
[TBL] [Abstract][Full Text] [Related]
27. Changing family structure in a modernizing society: a study of marriage patterns in a single Muslim village in Israel.
Zlotogora J; Habiballa H; Odatalla A; Barges S
Am J Hum Biol; 2002; 14(5):680-2. PubMed ID: 12203822
[TBL] [Abstract][Full Text] [Related]
28. Consanguinity among the Arab and Jewish populations in Israel.
Jaber L; Halpern GJ
Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():437-46. PubMed ID: 17551463
[TBL] [Abstract][Full Text] [Related]
29. A family with three recessive traits and homozygosity for a long 9qh+ chromosome segment.
Christian JC; Dexter RN; Palmer CG; Muller J
Am J Med Genet; 1980; 6(4):301-8. PubMed ID: 6938130
[TBL] [Abstract][Full Text] [Related]
30. Effects of consanguineous marriages on morbidity and precocious mortality: genetic counseling.
Freire-Maia N
Am J Med Genet; 1984 Jul; 18(3):401-6. PubMed ID: 6476000
[TBL] [Abstract][Full Text] [Related]
31. High incidence of profound deafness in an isolated community.
Zlotogora J; Barges S
Genet Test; 2003; 7(2):143-5. PubMed ID: 12885337
[TBL] [Abstract][Full Text] [Related]
32. [The impact of prenatal diagnosis on the prevention of chromosomal mental retardation. Chromosomal alterations that can be detected by prenatal diagnosis].
Soler-Casas A; Sánchez-Díaz A; Morales-Peydró C
Rev Neurol; 2006 Jan; 42 Suppl 1():S27-32. PubMed ID: 16506129
[TBL] [Abstract][Full Text] [Related]
33. Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?
Fares F; Badarneh K; Abosaleh M; Harari-Shaham A; Diukman R; David M
Prenat Diagn; 2008 Mar; 28(3):236-41. PubMed ID: 18264947
[TBL] [Abstract][Full Text] [Related]
34. [A comprehensive program for prevention of genetic diseases among Arabs in Israel].
Shalev SA; Carmi R; Leventhal A; Zlotogora J
Harefuah; 2003 Nov; 142(11):792-4, 804. PubMed ID: 14631914
[TBL] [Abstract][Full Text] [Related]
35. Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRT2A).
Higgins JJ; Pucilowska J; Lombardi RQ; Rooney JP
Clin Genet; 2004 Jun; 65(6):496-500. PubMed ID: 15151510
[TBL] [Abstract][Full Text] [Related]
36. Prevention of beta-thalassemia in a large Pakistani family through cascade testing.
Baig SM; Din MA; Hassan H; Azhar A; Baig JM; Aslam M; Anjum I; Farooq M; Hussain MS; Rasool M; Nawaz S; Qureshi JA; Zaman T
Community Genet; 2008; 11(1):68-70. PubMed ID: 18196920
[TBL] [Abstract][Full Text] [Related]
37. [Active screening for genetic pathology in newborns. II. Genetic counseling and prenatal diagnosis in high risk families].
Kovacheva K; Angelova L; Simeonova M
Akush Ginekol (Sofiia); 2004; 43(5):32-5. PubMed ID: 15518282
[TBL] [Abstract][Full Text] [Related]
38. A community genetics approach to population screening in India for mental retardation--a model for developing countries.
Dave U; Shetty N; Mehta L
Ann Hum Biol; 2005; 32(2):195-203. PubMed ID: 16096217
[TBL] [Abstract][Full Text] [Related]
39. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
Cohen D; Bar-Yosef U; Levy J; Gradstein L; Belfair N; Ofir R; Joshua S; Lifshitz T; Carmi R; Birk OS
Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
[TBL] [Abstract][Full Text] [Related]
40. [Medico-genetic consultation of families of oligophrenic patients (according to empirical risk findings)].
Danielov MB; Utin AV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1985; 85(3):394-8. PubMed ID: 3993300
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
