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Journal Abstract Search
127 related items for PubMed ID: 1605233
21. Marker X-associated mental retardation. A study of 150 retarded males. Kähkönen M, Leisti J, Wilska M, Varonen S. Clin Genet; 1983 Jun; 23(6):397-404. PubMed ID: 6576874 [Abstract] [Full Text] [Related]
23. Conference report: International Workshop on the fragile X and X-linked mental retardation. Opitz JM, Sutherland GR. Am J Med Genet; 1984 Jan; 17(1):5-94. PubMed ID: 6369987 [No Abstract] [Full Text] [Related]
24. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability. Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M. Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283 [Abstract] [Full Text] [Related]
25. Homicide, fragile X syndrome, and mental retardation. Telles LE, Zoratto PH, Day VP, Rosa RF. Braz J Psychiatry; 2013 Apr; 35(4):443-4. PubMed ID: 24402223 [No Abstract] [Full Text] [Related]
28. [Mental retardation in fragile X syndrome]. Mandel JL, Biancalana V, Cossée M, Devys D, Moutou C. Arch Pediatr; 1996 Apr; 3 Suppl 1():349s-350s. PubMed ID: 8796076 [No Abstract] [Full Text] [Related]
29. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Oberlé I, Camerino G, Wrogemann K, Arveiler B, Hanauer A, Raimondi E, Mandel JL. Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701 [Abstract] [Full Text] [Related]
30. Linkage and recombination between fragile X-linked mental retardation and the factor IX gene. Warren ST, Glover TW, Davidson RL, Jagadeeswaran P. Hum Genet; 1985 Sep; 69(1):44-6. PubMed ID: 3967889 [Abstract] [Full Text] [Related]
31. [Phenotypic screening for X-linked mental retardation: fragile Xq syndrome]. Lacassie I, Zavala AB, Curotto B, Alliende MA, De Andraca I. Rev Chil Pediatr; 1982 Sep; 53(5):419-25. PubMed ID: 7182864 [No Abstract] [Full Text] [Related]
32. A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome. Demirhan O, Taştemir D, Diler RS, Firat S, Avci A. Yonsei Med J; 2003 Aug 30; 44(4):583-92. PubMed ID: 12950112 [Abstract] [Full Text] [Related]
33. [Molecular pathogenesis of fragile X syndrome]. Sielska D, Milewski M, Bal J. Med Wieku Rozwoj; 2002 Aug 30; 6(4):295-308. PubMed ID: 12810982 [Abstract] [Full Text] [Related]