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2. Mental retardation in Nance-Horan syndrome: clinical and neuropsychological assessment in four families. Toutain A; Ayrault AD; Moraine C Am J Med Genet; 1997 Aug; 71(3):305-14. PubMed ID: 9268101 [TBL] [Abstract][Full Text] [Related]
3. Two sisters with mental retardation, cataract, ataxia, progressive hearing loss, and polyneuropathy. Begeer JH; Scholte FA; van Essen AJ J Med Genet; 1991 Dec; 28(12):884-5. PubMed ID: 1661780 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Is there an X-linked form of congenital cataracts? Crews SJ; Bundey SE Clin Genet; 1982 May; 21(5):351-3. PubMed ID: 7116682 [No Abstract] [Full Text] [Related]
7. Classification of hereditary cataracts in children by linkage analysis. Maumenee IH Ophthalmology; 1979 Sep; 86(9):1554-8. PubMed ID: 121767 [TBL] [Abstract][Full Text] [Related]
8. X-linked mental retardation without physical abnormality: Renpenning's syndrome. Turner G; Turner B; Collins E Dev Med Child Neurol; 1971 Feb; 13(1):71-8. PubMed ID: 4929082 [No Abstract] [Full Text] [Related]
9. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report. Mattei JF; Collignon P; Ayme S; Giraud F Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021 [No Abstract] [Full Text] [Related]
10. 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]
12. X linked mental retardation: a family with a separate syndrome? Thompson EM; Gordon A; Baraitser M J Med Genet; 1989 Jun; 26(6):373-8. PubMed ID: 2738899 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11. Reyniers E; Van Bogaert P; Peeters N; Vits L; Pauly F; Fransen E; Van Regemorter N; Kooy RF Am J Hum Genet; 1999 Nov; 65(5):1406-12. PubMed ID: 10521307 [TBL] [Abstract][Full Text] [Related]
16. Fragile X syndrome: a major cause of X-linked mental retardation. Butler MG Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303 [No Abstract] [Full Text] [Related]
17. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome. Seemanová E; Lesný I Am J Med Genet; 1996 Dec; 66(2):179-83. PubMed ID: 8958326 [TBL] [Abstract][Full Text] [Related]
18. Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism. Sutherland GR; Judge CG; Wiener S J Med Genet; 1980 Feb; 17(1):73-4. PubMed ID: 7189219 [No Abstract] [Full Text] [Related]
19. A novel Xp22.13 microdeletion in Nance-Horan syndrome. Accogli A; Traverso M; Madia F; Bellini T; Vari MS; Pinto F; Capra V Birth Defects Res; 2017 Jul; 109(11):866-868. PubMed ID: 28464487 [TBL] [Abstract][Full Text] [Related]