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Journal Abstract Search
262 related items for PubMed ID: 6885061
1. Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother. Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H. Hum Genet; 1983; 64(2):196-9. PubMed ID: 6885061 [Abstract] [Full Text] [Related]
2. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome. Schmidt M, Certoma A, Du Sart D, Kalitsis P, Leversha M, Fowler K, Sheffield L, Jack I, Danks DM. Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456 [Abstract] [Full Text] [Related]
5. Choroideremia in interstitial deletion of the X chromosome. Rosenberg T, Schwartz M, Niebuhr E, Yang HM, Sardemann H, Andersen O, Lundsteen C. Ophthalmic Paediatr Genet; 1986 Dec; 7(3):205-10. PubMed ID: 2882458 [Abstract] [Full Text] [Related]
7. Duplication of the short arm of the X chromosome in mother and daughter. Tuck-Muller CM, Martinez JE, Batista DA, Kearns WG, Wertelecki W. Hum Genet; 1993 May; 91(4):395-400. PubMed ID: 8500796 [Abstract] [Full Text] [Related]
11. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation. Silengo MC, Luzzatti L, Centerwall WR, Costello JM, Parslow M. Clin Genet; 1981 Mar; 19(3):174-80. PubMed ID: 7273460 [Abstract] [Full Text] [Related]
17. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15). Stoll C, Levy J, Roth MP. J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434 [Abstract] [Full Text] [Related]
18. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Ballabio A, Bardoni B, Carrozzo R, Andria G, Bick D, Campbell L, Hamel B, Ferguson-Smith MA, Gimelli G, Fraccaro M. Proc Natl Acad Sci U S A; 1989 Dec; 86(24):10001-5. PubMed ID: 2602357 [Abstract] [Full Text] [Related]