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7. 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]
8. X-linked mental retardation with dystonic movements of the hands. Partington MW; Mulley JC; Sutherland GR; Hockey A; Thode A; Turner G Am J Med Genet; 1988; 30(1-2):251-62. PubMed ID: 3177452 [TBL] [Abstract][Full Text] [Related]
9. Radiographic features of spondylo-epimetaphyseal dysplasia with joint laxity and progressive kyphoscoliosis. Review of 19 cases. Kozlowski K; Beighton P Rofo; 1984 Sep; 141(3):337-41. PubMed ID: 6435203 [TBL] [Abstract][Full Text] [Related]
10. A new X-linked mental retardation syndrome. Homfray T; Holland T; Patton M Clin Dysmorphol; 1995 Oct; 4(4):289-93. PubMed ID: 8574418 [TBL] [Abstract][Full Text] [Related]
11. The manifestations and natural history of spondylo-epi-metaphyseal dysplasia with joint laxity. Beighton P; Gericke G; Kozlowski K; Grobler L Clin Genet; 1984 Oct; 26(4):308-17. PubMed ID: 6499247 [TBL] [Abstract][Full Text] [Related]
12. A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous family. Yasin S; Mustafa S; Ayesha A; Latif M; Hassan M; Faisal M; Makitie O; Iqbal F; Naz S Eur J Med Genet; 2020 Aug; 63(8):103958. PubMed ID: 32470407 [TBL] [Abstract][Full Text] [Related]
13. Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3. Kozák L; Chiurazzi P; Genuardi M; Pomponi MG; Zollino M; Neri G J Med Genet; 1993 Oct; 30(10):866-9. PubMed ID: 8230164 [TBL] [Abstract][Full Text] [Related]
15. [Genetic study of eight cases of spondylo-epiphyseal dysplasia tarda and its autosomal recessive transmission]. Chaabouni H; Douiri H; Abdelkefi MM; Miladi M; Slimane N; Ferchiou A J Genet Hum; 1986 Aug; 34(3-4):275-84. PubMed ID: 3760831 [TBL] [Abstract][Full Text] [Related]
16. Linkage to Xq28 in a family with nonspecific X-linked mental retardation. Nordström AM; Penttinen M; von Koskull H Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558 [TBL] [Abstract][Full Text] [Related]
17. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22. Strain L; Wright AF; Bonthron DT J Med Genet; 1997 Jul; 34(7):535-40. PubMed ID: 9222959 [TBL] [Abstract][Full Text] [Related]
18. X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males. Wilkie AO; Gibbons RJ; Higgs DR; Pembrey ME J Med Genet; 1991 Nov; 28(11):738-41. PubMed ID: 1770529 [TBL] [Abstract][Full Text] [Related]
20. A new X linked syndrome with mental retardation and craniofacial dysmorphism? Hyde-Forster I; McCarthy G; Berry AC J Med Genet; 1992 Oct; 29(10):736-8. PubMed ID: 1433236 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]