These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
118 related articles for article (PubMed ID: 3177474)
21. Inheritance of fragile X syndrome: an hypothesis. Friedman JM; Howard-Peebles PN Am J Med Genet; 1986; 23(1-2):701-13. PubMed ID: 3006493 [TBL] [Abstract][Full Text] [Related]
22. The fragile X syndrome: variability of expression in carrier females. Howard-Peebles PN; Brown WT Am J Med Genet; 1988; 30(1-2):227-30. PubMed ID: 3177448 [TBL] [Abstract][Full Text] [Related]
23. Genetics and expression of the fragile X syndrome. Brown WT; Jenkins EC; Gross AC; Chan CB; Wisniewski K; Cohen IL; Miezejeski CM Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523 [TBL] [Abstract][Full Text] [Related]
24. Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype. Steinbach P; Barbi G; Baur S; Vogel W Hum Genet; 1983; 64(3):279-82. PubMed ID: 6885072 [TBL] [Abstract][Full Text] [Related]
25. Twin births to mothers who are twins: a registry based study. Lichtenstein P; Olausson PO; Källén AJ BMJ; 1996 Apr; 312(7035):879-81. PubMed ID: 8611875 [TBL] [Abstract][Full Text] [Related]
26. Further evidence for genetic heterogeneity in the fragile X syndrome. Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105 [TBL] [Abstract][Full Text] [Related]
27. Fragile X mutation and FG syndrome-like phenotype. Piussan C; Mathieu M; Berquin P; Fryns JP Am J Med Genet; 1996 Aug; 64(2):395-8. PubMed ID: 8844090 [TBL] [Abstract][Full Text] [Related]
28. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome. Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280 [TBL] [Abstract][Full Text] [Related]
29. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity. Brown WT; Gross AC; Chan CB; Jenkins EC Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490 [TBL] [Abstract][Full Text] [Related]
30. Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex. Costa T; Lambert M; Teshima I; Ray PN; Richer CL; Dallaire L Am J Med Genet; 1998 Jan; 75(1):40-4. PubMed ID: 9450855 [TBL] [Abstract][Full Text] [Related]
32. X inactivation patterns in female monozygotic twins and their families. Watkiss E; Webb T; Rysiecki G; Girdler N; Hewett E; Bundey S J Med Genet; 1994 Oct; 31(10):754-7. PubMed ID: 7837250 [TBL] [Abstract][Full Text] [Related]
33. Selective advantage of fra (X) heterozygotes. Vogel F; Crusio WE; Kovac C; Fryns JP; Freund M Hum Genet; 1990 Nov; 86(1):25-32. PubMed ID: 2147668 [TBL] [Abstract][Full Text] [Related]
34. Prenatal detection of fra(X)(q27.3) in female identical twins: reliability of low level cytogenetic prenatal expression in females. Jenkins EC; Brown WT; Schonberg S; Krawczun MS; Goldberg J; Golbus MS Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):128-35. PubMed ID: 1605181 [TBL] [Abstract][Full Text] [Related]
35. Recurrence risks for relatives in families with an isolated case of the fragile X syndrome. Sherman SL; Rogatko A; Turner G Am J Med Genet; 1988 Dec; 31(4):753-65. PubMed ID: 3239564 [TBL] [Abstract][Full Text] [Related]
36. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males. Soudek D; Partington MW; Lawson JS Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598 [TBL] [Abstract][Full Text] [Related]
37. The strength of association between fragile (X) chromosome presence and mental retardation. Silverman W; Lubin R; Jenkins EC; Brown WT Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008 [TBL] [Abstract][Full Text] [Related]
38. Methylation and mutation patterns in the fragile X syndrome. Malmgren H; Steén-Bondeson ML; Gustavson KH; Seémanova E; Holmgren G; Oberlé I; Mandel JL; Pettersson U; Dahl N Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):268-78. PubMed ID: 1605200 [TBL] [Abstract][Full Text] [Related]
39. Is hemifacial microsomia linked to multiple maternities? Lawson K; Waterhouse N; Gault DT; Calvert ML; Botma M; Ng R Br J Plast Surg; 2002 Sep; 55(6):474-8. PubMed ID: 12479420 [TBL] [Abstract][Full Text] [Related]