121 related articles for article (PubMed ID: 18446860)
1. Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
Nolan DK; Chen P; Das S; Ober C; Waggoner D
Am J Med Genet A; 2008 Jun; 146A(11):1414-22. PubMed ID: 18446860
[TBL] [Abstract][Full Text] [Related]
2. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.
Basel-Vanagaite L; Attia R; Yahav M; Ferland RJ; Anteki L; Walsh CA; Olender T; Straussberg R; Magal N; Taub E; Drasinover V; Alkelai A; Bercovich D; Rechavi G; Simon AJ; Shohat M
J Med Genet; 2006 Mar; 43(3):203-10. PubMed ID: 16033914
[TBL] [Abstract][Full Text] [Related]
3. Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.
Basel-Vanagaite L; Alkelai A; Straussberg R; Magal N; Inbar D; Mahajna M; Shohat M
J Med Genet; 2003 Oct; 40(10):729-32. PubMed ID: 14569116
[TBL] [Abstract][Full Text] [Related]
4. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.
Uyguner O; Kayserili H; Li Y; Karaman B; Nürnberg G; Hennies H; Becker C; Nürnberg P; Başaran S; Apak MY; Wollnik B
Clin Genet; 2007 Mar; 71(3):212-9. PubMed ID: 17309643
[TBL] [Abstract][Full Text] [Related]
5. A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter.
Higgins JJ; Rosen DR; Loveless JM; Clyman JC; Grau MJ
Neurology; 2000 Aug; 55(3):335-40. PubMed ID: 10932263
[TBL] [Abstract][Full Text] [Related]
6. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
Noor A; Windpassinger C; Patel M; Stachowiak B; Mikhailov A; Azam M; Irfan M; Siddiqui ZK; Naeem F; Paterson AD; Lutfullah M; Vincent JB; Ayub M
Am J Hum Genet; 2008 Apr; 82(4):1011-8. PubMed ID: 18387594
[TBL] [Abstract][Full Text] [Related]
7. DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
Santos RL; Hassan MJ; Sikandar S; Lee K; Ali G; Martin PE; Wambangco MA; Ahmad W; Leal SM
Hum Genet; 2006 Aug; 120(1):85-92. PubMed ID: 16703383
[TBL] [Abstract][Full Text] [Related]
8. Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
Çalışkan M; Chong JX; Uricchio L; Anderson R; Chen P; Sougnez C; Garimella K; Gabriel SB; dePristo MA; Shakir K; Matern D; Das S; Waggoner D; Nicolae DL; Ober C
Hum Mol Genet; 2011 Apr; 20(7):1285-9. PubMed ID: 21212097
[TBL] [Abstract][Full Text] [Related]
9. [Linkage analysis of six Algerian families with autosomal recessive non specific mental retardation].
Guessibia N; Sarrai N; Methari N; Ridouh B; Chaabouni Bouhamed H
Tunis Med; 2011 May; 89(5):466-70. PubMed ID: 21557185
[TBL] [Abstract][Full Text] [Related]
10. A locus for autosomal recessive idiopathic hypogonadotropic hypogonadism on chromosome 19p13.3.
Acierno JS; Shagoury JK; Bo-Abbas Y; Crowley WF; Seminara SB
J Clin Endocrinol Metab; 2003 Jun; 88(6):2947-50. PubMed ID: 12788910
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
Martínez F; Martínez-Garay I; Oltra S; Moltó MD; Orellana C; Monfort S; Prieto F; Tejada I
Am J Med Genet A; 2004 Dec; 131(2):174-8. PubMed ID: 15526294
[TBL] [Abstract][Full Text] [Related]
13. Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel.
Rehman Su; Baig SM; Eiberg H; Rehman Su; Ahmad I; Malik NA; Tommerup N; Hansen L
Neurogenetics; 2011 Aug; 12(3):247-51. PubMed ID: 21643797
[TBL] [Abstract][Full Text] [Related]
14. Fine mapping of MRT9 locus through genome wide homozygosity mapping in a consanguineous Pakistani family.
Rehman SU; Baig SM; Hasen L; Ahmad I; Khan RA; Hussa M
J Pak Med Assoc; 2019 Dec; 69(12):1903-1906. PubMed ID: 31853126
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
Riazuddin SA; Yasmeen A; Zhang Q; Yao W; Sabar MF; Ahmed Z; Riazuddin S; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):623-6. PubMed ID: 15671291
[TBL] [Abstract][Full Text] [Related]
17. A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.
Smaoui N; Beltaief O; BenHamed S; M'Rad R; Maazoul F; Ouertani A; Chaabouni H; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2716-21. PubMed ID: 15277496
[TBL] [Abstract][Full Text] [Related]
18. A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.
Skehan EB; Abdulrahim MM; Parfrey NA; Hand CK
Neurogenetics; 2012 May; 13(2):125-32. PubMed ID: 22411506
[TBL] [Abstract][Full Text] [Related]
19. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
Ain Q; Nazli S; Riazuddin S; Jaleel AU; Riazuddin SA; Zafar AU; Khan SN; Husnain T; Griffith AJ; Ahmed ZM; Friedman TB; Riazuddin S
Hum Genet; 2007 Dec; 122(5):445-50. PubMed ID: 17690910
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
