110 related articles for article (PubMed ID: 3953642)
1. X-linked intellectual handicap and precocious puberty with obesity in carrier females.
Hockey A
Am J Med Genet; 1986; 23(1-2):127-37. PubMed ID: 3953642
[TBL] [Abstract][Full Text] [Related]
2. X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.
Nielsen KB; Tommerup N; Poulsen H; Mikkelsen M
Hum Genet; 1981; 59(1):23-5. PubMed ID: 10819017
[TBL] [Abstract][Full Text] [Related]
3. Familial spastic paraplegia, mental retardation, and precocious puberty.
Raphaelson MI; Stevens JC; Elders J; Comite F; Theodore WH
Arch Neurol; 1983 Dec; 40(13):809-10. PubMed ID: 6639408
[TBL] [Abstract][Full Text] [Related]
4. Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives.
Sutherland GR
Hum Genet; 1979; 53(1):23-7. PubMed ID: 535898
[TBL] [Abstract][Full Text] [Related]
5. A new syndrome with mental retardation, short stature and an Xq duplication.
Thode A; Partington MW; Yip MY; Chapman C; Richardson VF; Turner G
Am J Med Genet; 1988; 30(1-2):239-50. PubMed ID: 3177451
[TBL] [Abstract][Full Text] [Related]
6. New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum.
Proud VK; Levine C; Carpenter NJ
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):458-66. PubMed ID: 1605226
[TBL] [Abstract][Full Text] [Related]
7. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D
J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
[TBL] [Abstract][Full Text] [Related]
8. Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.
Gustavson KH; Holmgren G; Blomquist HK; Mikkelsen M; Nordenson I; Poulsen H; Tommerup N
Clin Genet; 1981 Feb; 19(2):101-10. PubMed ID: 7193540
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
de Vries BB; Fryns JP; Butler MG; Canziani F; Wesby-van Swaay E; van Hemel JO; Oostra BA; Halley DJ; Niermeijer MF
J Med Genet; 1993 Sep; 30(9):761-6. PubMed ID: 8411072
[TBL] [Abstract][Full Text] [Related]
10. Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.
Kondo I; Hamabe J; Yamamoto K; Niikawa N
Clin Genet; 1990 Dec; 38(6):422-6. PubMed ID: 1981180
[TBL] [Abstract][Full Text] [Related]
11. Duplication or insertion in 15q11-13 associated with mental retardation-short stature and obesity-Prader-Willi or Cohen syndrome?
Fuhrmann-Rieger A; Köhler A; Fuhrmann W
Clin Genet; 1984 Apr; 25(4):347-52. PubMed ID: 6713711
[TBL] [Abstract][Full Text] [Related]
12. The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.
Donnai D; Clayton-Smith J; Gibbons RJ; Higgs DR
J Med Genet; 1991 Nov; 28(11):742-5. PubMed ID: 1770530
[TBL] [Abstract][Full Text] [Related]
13. An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion.
Lybaek H; Ørstavik KH; Prescott T; Hovland R; Breilid H; Stansberg C; Steen VM; Houge G
Eur J Hum Genet; 2009 Jul; 17(7):904-10. PubMed ID: 19156171
[TBL] [Abstract][Full Text] [Related]
14. Linkage analysis in a large family with nonspecific X-linked mental retardation.
Glass IA; White EM; Pope MJ; Pirrit LA; Cockburn F; Connor JM
Am J Med Genet; 1991; 38(2-3):240-3. PubMed ID: 1673298
[TBL] [Abstract][Full Text] [Related]
15. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
Proops R; Webb T
J Med Genet; 1981 Oct; 18(5):366-73. PubMed ID: 7328617
[TBL] [Abstract][Full Text] [Related]
16. Precocious puberty in the male offspring of a mother and daughter with the Prader-Willi syndrome.
Hockey A; Byrne G; Cohen A
Am J Med Genet; 1987 Mar; 26(3):749. PubMed ID: 3565489
[No Abstract] [Full Text] [Related]
17. Familial early puberty: presentation and inheritance pattern in 139 families.
Durand A; Bashamboo A; McElreavey K; Brauner R
BMC Endocr Disord; 2016 Sep; 16(1):50. PubMed ID: 27624871
[TBL] [Abstract][Full Text] [Related]
18. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
Fishburn J; Turner G; Daniel A; Brookwell R
Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625
[TBL] [Abstract][Full Text] [Related]
19. X-linked mental retardation with the fragile X. A study of 15 families.
Mattei JF; Mattei MG; Aumeras C; Auger M; Giraud F
Hum Genet; 1981; 59(4):281-9. PubMed ID: 7333582
[TBL] [Abstract][Full Text] [Related]
20. X-linked mental retardation associated with psoriasis: a new syndrome?
Tranebjaerg L; Svejgaard A; Lykkesfeldt G
Am J Med Genet; 1988; 30(1-2):263-73. PubMed ID: 3177453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]