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3. [Progress in pediatric neurology]. Landrieu P Rev Neurol (Paris); 2000 Jul; 156(6-7):595-605. PubMed ID: 10891793 [TBL] [Abstract][Full Text] [Related]
4. New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death. Gustavson KH; Annerén G; Malmgren H; Dahl N; Ljunggren CG; Bäckman H Am J Med Genet; 1993 Mar; 45(5):654-8. PubMed ID: 8456840 [TBL] [Abstract][Full Text] [Related]
5. Molecular genetics of the X chromosome and X-linked diseases. Craig IW; Goodfellow PN Lab Invest; 1986 Mar; 54(3):241-53. PubMed ID: 3512907 [No Abstract] [Full Text] [Related]
6. XLMR genes: update 1994. Neri G; Chiurazzi P; Arena JF; Lubs HA Am J Med Genet; 1994 Jul; 51(4):542-9. PubMed ID: 7943038 [TBL] [Abstract][Full Text] [Related]
7. Sixty years of X-linked mental retardation: a historical footnote. Neri G; Opitz JM Am J Med Genet; 2000; 97(3):228-33. PubMed ID: 11449492 [TBL] [Abstract][Full Text] [Related]
9. Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2. Bar-David S; Lerer I; Sarfaty CK; Kohan ZG; Meiner V; Zlotogora J; Abeliovich D Am J Med Genet; 1996 Jul; 64(1):83-8. PubMed ID: 8826456 [TBL] [Abstract][Full Text] [Related]
10. Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31. Shrimpton AE; Daly KM; Hoo JJ Am J Med Genet; 1999 May; 84(3):293-9. PubMed ID: 10331611 [TBL] [Abstract][Full Text] [Related]
11. Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22. Donnelly AJ; Choo KH; Kozman HM; Gedeon AK; Danks DM; Mulley JC Am J Med Genet; 1994 Jul; 51(4):581-5. PubMed ID: 7943043 [TBL] [Abstract][Full Text] [Related]
12. Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome. Gedeon AK; Kozman HM; Robinson H; Pilia G; Schlessinger D; Turner G; Mulley JC Am J Med Genet; 1996 Jul; 64(1):63-8. PubMed ID: 8826450 [TBL] [Abstract][Full Text] [Related]
13. A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28. Hamel BC; Kremer H; Wesby-van Swaay E; van den Helm B; Smits AP; Oostra BA; Ropers HH; Mariman EC Am J Med Genet; 1996 Jul; 64(1):131-3. PubMed ID: 8826463 [TBL] [Abstract][Full Text] [Related]
14. Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38). Schutz CK; Ives EJ; Chalifoux M; MacLaren L; Farrell S; Robinson PD; White BN; Holden JJ Am J Med Genet; 1996 Jul; 64(1):89-96. PubMed ID: 8826457 [TBL] [Abstract][Full Text] [Related]
15. X-linked alpha-thalassemia/mental retardation syndrome. Linkage analysis in a new family further supports localization in proximal Xq. Houdayer CI; Toutain A; Ronce N; Lefort G; Sarda P; Taib J; Briault S; Lambert JC; Moraine CI Ann Genet; 1993; 36(4):194-9. PubMed ID: 8166423 [TBL] [Abstract][Full Text] [Related]
16. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation. Gedeon AK; Glass IA; Connor JM; Mulley JC Am J Med Genet; 1996 Jul; 64(1):121-4. PubMed ID: 8826461 [TBL] [Abstract][Full Text] [Related]
17. [Mental retardation and hereditary enzymopathy (review)]. D'iachkova AIa; Lebedev BV Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1588-93. PubMed ID: 5003148 [No Abstract] [Full Text] [Related]
18. [3 examples of fetal genetic neuromuscular disorders which lead to hydramnion]. Teeuw AH; Barth PG; van Sonderen L; Zondervan HA Ned Tijdschr Geneeskd; 1993 May; 137(18):908-13. PubMed ID: 8492834 [TBL] [Abstract][Full Text] [Related]
19. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene. Biancalana V; Trivier E; Weber C; Weissenbach J; Rowe PS; O'Riordan JL; Partington MW; Heyberger S; Oudet C; Hanauer A Genomics; 1994 Aug; 22(3):617-25. PubMed ID: 8001973 [TBL] [Abstract][Full Text] [Related]
20. Splitting and lumping in the nosology of XLMR. Stevenson RE Am J Med Genet; 2000; 97(3):174-82. PubMed ID: 11449485 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]