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22. Investigation of the twinning rate in families with the fragile X syndrome. Sherman SL, Turner G, Sheffield L, Laing S, Robinson H. Am J Med Genet; 1988; 30(1-2):625-31. PubMed ID: 3177474 [Abstract] [Full Text] [Related]
25. Sex chromosome aneuploidy in fragile X carriers. Nielsen KB. Am J Med Genet; 1986; 23(1-2):537-44. PubMed ID: 3953664 [Abstract] [Full Text] [Related]
29. [Mental retardation with X fragility: Armenfrax. Review and personal studies]. Engel E. Rev Med Suisse Romande; 1983 Apr; 103(4):333-44. PubMed ID: 6348915 [No Abstract] [Full Text] [Related]
30. The fragile X syndrome: variability of expression in carrier females. Howard-Peebles PN, Brown WT. Am J Med Genet; 1988 Apr; 30(1-2):227-30. PubMed ID: 3177448 [Abstract] [Full Text] [Related]
32. Clinical features and reproductive patterns in fragile X female heterozygotes. Loesch DZ, Hay DA. J Med Genet; 1988 Jun; 25(6):407-14. PubMed ID: 3398009 [Abstract] [Full Text] [Related]
38. Fragile X transmission and the determination of carrier probabilities for genetic counseling. Mulley JC, Sutherland GR. Am J Med Genet; 1987 Apr; 26(4):987-90. PubMed ID: 3591842 [No Abstract] [Full Text] [Related]
40. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation. Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF. Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]