These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
109 related articles for article (PubMed ID: 7943040)
1. X-linked mental retardation with dystonic movements of the hands (PRTS): revisited. Gedeon A; Partington M; Mulley J Am J Med Genet; 1994 Jul; 51(4):565-8. PubMed ID: 7943040 [TBL] [Abstract][Full Text] [Related]
2. Clinical study and haplotype analysis in two brothers with Partington syndrome. Frints SG; Borghgraef M; Froyen G; Marynen P; Fryns JP Am J Med Genet; 2002 Nov; 112(4):361-8. PubMed ID: 12376938 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited. Hu LJ; Blumenfeld-Heyberger S; Hanauer A; Weissenbach J; Mandel JL Am J Med Genet; 1994 Jul; 51(4):569-74. PubMed ID: 7943041 [TBL] [Abstract][Full Text] [Related]
7. X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization. Turner G; Gedeon A; Mulley J Am J Med Genet; 1994 Jul; 51(4):575-80. PubMed ID: 7943042 [TBL] [Abstract][Full Text] [Related]
8. Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation. Turner G; Partington M; Kerr B; Mangelsdorf M; Gecz J Am J Med Genet; 2002 Nov; 112(4):405-11. PubMed ID: 12376946 [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. Pericentromeric genes for non-specific X-linked mental retardation (MRX). Gedeon A; Kerr B; Mulley J; Turner G Am J Med Genet; 1994 Jul; 51(4):553-64. PubMed ID: 7943039 [TBL] [Abstract][Full Text] [Related]
11. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). Holinski-Feder E; Golla A; Rost I; Seidel H; Rittinger O; Meindl A Am J Med Genet; 1996 Jul; 64(1):125-30. PubMed ID: 8826462 [TBL] [Abstract][Full Text] [Related]
12. Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3. MartÃnez F; Gal A; Palau F; Prieto F Am J Med Genet; 1995 Jan; 55(3):387-90. PubMed ID: 7726242 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50). Claes S; Vogels A; Holvoet M; Devriendt K; Raeymaekers P; Cassiman JJ; Fryns JP Am J Med Genet; 1997 Dec; 73(4):474-9. PubMed ID: 9415477 [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. A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11. Deqaqi SC; N'Guessan M; Forner J; Sbiti A; Beldjord C; Chelly J; Sefiani A; Des Portes V Ann Genet; 1998; 41(1):11-6. PubMed ID: 9599645 [TBL] [Abstract][Full Text] [Related]
18. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21. Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]