144 related articles for article (PubMed ID: 10398239)
1. X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23.
Chudley AE; Tackels DC; Lubs HA; Arena JF; Stoeber WP; Kovnats S; Stevenson RE; Schwartz CE
Am J Med Genet; 1999 Jul; 85(3):255-62. PubMed ID: 10398239
[TBL] [Abstract][Full Text] [Related]
2. Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.
des Portes V; Soufir N; Carrié A; Billuart P; Bienvenu T; Vinet MC; Beldjord C; Ponsot G; Kahn A; Boué J; Chelly J
Am J Med Genet; 1997 Oct; 72(3):324-8. PubMed ID: 9332663
[TBL] [Abstract][Full Text] [Related]
3. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
Carpenter NJ; Qu Y; Curtis M; Patil SR
Am J Med Genet; 1999 Jul; 85(3):230-5. PubMed ID: 10398234
[TBL] [Abstract][Full Text] [Related]
4. X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.
Abidi F; Hall BD; Cadle RG; Feldman GL; Lubs HA; Ouzts LV; Arena JF; Stevenson RE; Schwartz CE
Am J Med Genet; 1999 Jul; 85(3):223-9. PubMed ID: 10398233
[TBL] [Abstract][Full Text] [Related]
5. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
Armfield K; Nelson R; Lubs HA; Häne B; Schroer RJ; Arena F; Schwartz CE; Stevenson RE
Am J Med Genet; 1999 Jul; 85(3):236-42. PubMed ID: 10398235
[TBL] [Abstract][Full Text] [Related]
6. Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22.
Häne B; Stevenson RE; Arena JF; Lubs HA; Simensen RJ; Schwartz CE
Am J Med Genet; 1999 Jul; 85(3):271-5. PubMed ID: 10398242
[TBL] [Abstract][Full Text] [Related]
7. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
Schwartz CE; Ulmer J; Brown A; Pancoast I; Goodman HO; Stevenson RE
Am J Hum Genet; 1990 Sep; 47(3):454-8. PubMed ID: 2393020
[TBL] [Abstract][Full Text] [Related]
8. Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
Holinski-Feder E; Chahrockh-Zadeh S; Rittinger O; Jedele KB; Gasteiger M; Lenski C; Murken J; Golla A
Am J Med Genet; 1999 Sep; 86(2):102-6. PubMed ID: 10449641
[TBL] [Abstract][Full Text] [Related]
9. Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21.
Badenas C; Castellví-Bel S; Volpini V; Jiménez D; Sánchez A; Estivill X; Milà M
Am J Med Genet; 2001 Feb; 98(4):343-7. PubMed ID: 11170079
[TBL] [Abstract][Full Text] [Related]
10. A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.
Cabezas DA; Slaugh R; Abidi F; Arena JF; Stevenson RE; Schwartz CE; Lubs HA
J Med Genet; 2000 Sep; 37(9):663-8. PubMed ID: 10978355
[TBL] [Abstract][Full Text] [Related]
11. Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54).
Jemaa LB; des Portes V; Zemni R; Mrad R; Maazoul F; Beldjord C; Chaabouni H; Chelly J
Am J Med Genet; 1999 Jul; 85(3):276-82. PubMed ID: 10398243
[TBL] [Abstract][Full Text] [Related]
12. Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.
Ahmad W; De Fusco M; Faiyaz ul Haque M; Aridon P; Sarno T; Sohail M; ul Haque S; Ahmad M; Ballabio A; Franco B; Casari G
Eur J Hum Genet; 1999; 7(7):828-32. PubMed ID: 10573017
[TBL] [Abstract][Full Text] [Related]
13. X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region.
Yntema HG; van den Helm B; Knoers NV; Smits AP; van Roosmalen T; Smeets DF; Mariman EC; van der Burgt I; van Bokhoven H; Ropers HH; Kremer H; Hamel BC
Am J Med Genet; 1999 Jul; 85(3):305-8. PubMed ID: 10398247
[TBL] [Abstract][Full Text] [Related]
14. MRX8: an X-linked mental retardation condition with linkage to Xq21.
Schwartz CE; May M; Huang T; Ledbetter D; Anderson G; Barker DF; Lubs HA; Arena F; Stevenson RE
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):467-74. PubMed ID: 1605227
[TBL] [Abstract][Full Text] [Related]
15. Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.
Russo S; Cogliati F; Cavalleri F; Cassitto MG; Giglioli R; Toniolo D; Casari G; Larizza L
Am J Med Genet; 2000 Oct; 94(5):376-82. PubMed ID: 11050621
[TBL] [Abstract][Full Text] [Related]
16. Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.
Carpenter NJ; Brown WT; Qu Y; Keenan KL
Am J Med Genet; 1999 Jul; 85(3):266-70. PubMed ID: 10398241
[TBL] [Abstract][Full Text] [Related]
17. Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4.
Hedera P; Alvarado D; Beydoun A; Fink JK
Ann Neurol; 2002 Jan; 51(1):45-50. PubMed ID: 11782983
[TBL] [Abstract][Full Text] [Related]
18. Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
Martínez F; Martínez-Garay I; Millán JM; Pérez-Aytes A; Moltó MD; Orellana C; Prieto F
Am J Med Genet; 2001 Aug; 102(2):200-4. PubMed ID: 11477616
[TBL] [Abstract][Full Text] [Related]
19. Linkage of nonspecific X-linked mental retardation to Xq21.31.
Jedele KB; Michels VV; Schaid DJ; Schowalter KV; Thibodeau SN
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):436-42. PubMed ID: 1605223
[TBL] [Abstract][Full Text] [Related]
20. Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
Ahmad W; Noci S; Faiyaz ul Haque M; Sarno T; Aridon P; Ahmad MM; Amin-Ud-Din M; Rafiq MA; ul Haque S; De Fusco M; Ballabio A; Franco B; Casari G
Am J Med Genet; 2001 Apr; 100(1):62-5. PubMed ID: 11337751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
