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2. A novel locus for restless legs syndrome on chromosome 13q. Balaban H; Bayrakli F; Kartal U; Pinarbasi E; Topaktas S; Kars HZ Eur Neurol; 2012; 68(2):111-6. PubMed ID: 22797413 [TBL] [Abstract][Full Text] [Related]
3. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees. Basit S; Wali A; Aziz A; Muhammad N; Jelani M; Ahmad W Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890 [TBL] [Abstract][Full Text] [Related]
4. Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family. Kumar A; Shetty J; Kumar B; Blanton SH Mol Vis; 2004 Jun; 10():399-402. PubMed ID: 15215745 [TBL] [Abstract][Full Text] [Related]
5. Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21. Ali Mosrati M; Schrauwen I; Ben Saiid M; Aifa-Hmani M; Fransen E; Mneja M; Ghorbel A; Van Camp G; Masmoudi S J Hum Genet; 2013 Feb; 58(2):98-101. PubMed ID: 23235334 [TBL] [Abstract][Full Text] [Related]
6. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23. Stuhrmann M; Hennies HC; Bukhari IA; Brakensiek K; Nürnberg G; Becker C; Huebener J; Miranda MC; Frye-Boukhriss H; Knothe S; Schmidtke J; El-Harith EH Clin Genet; 2008 Jun; 73(6):566-72. PubMed ID: 18462451 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. Multiple extradural arachnoid cysts: report of two operated cousin cases. Yabuki S; Kikuchi S Spine (Phila Pa 1976); 2007 Sep; 32(20):E585-8. PubMed ID: 17873800 [TBL] [Abstract][Full Text] [Related]
9. The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15. Bilguvar K; Ozturk AK; Bayrakli F; Guzel A; DiLuna ML; Bayri Y; Tatli M; Tekes S; Arlier Z; Yasuno K; Mason CE; Lifton RP; State MW; Gunel M Am J Med Genet A; 2009 Nov; 149A(11):2569-72. PubMed ID: 19876906 [No Abstract] [Full Text] [Related]
10. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation. Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217 [TBL] [Abstract][Full Text] [Related]
13. Identification of an autosomal dominant locus for intracranial aneurysm through a model-based family collection in a geographically limited area. Kim CJ; Park SS; Lee HS; Chung HJ; Choi W; Chung JH; Kim JM; Hong ST J Hum Genet; 2011 Jun; 56(6):464-6. PubMed ID: 21451530 [TBL] [Abstract][Full Text] [Related]
14. Endoscopy versus microsurgical cyst excision and shunting for treating intracranial arachnoid cysts. Gangemi M; Seneca V; Colella G; Cioffi V; Imperato A; Maiuri F J Neurosurg Pediatr; 2011 Aug; 8(2):158-64. PubMed ID: 21806357 [TBL] [Abstract][Full Text] [Related]
15. Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Salzmann A; Guipponi M; Lyons PJ; Fricker LD; Sapio M; Lambercy C; Buresi C; Ouled Amar Bencheikh B; Lahjouji F; Ouazzani R; Crespel A; Chaigne D; Malafosse A Hum Mutat; 2012 Jan; 33(1):124-35. PubMed ID: 21922598 [TBL] [Abstract][Full Text] [Related]
16. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Othmane KB; Johnson E; Menold M; Graham FL; Hamida MB; Hasegawa O; Rogala AD; Ohnishi A; Pericak-Vance M; Hentati F; Vance JM Genomics; 1999 Dec; 62(3):344-9. PubMed ID: 10644431 [TBL] [Abstract][Full Text] [Related]
18. 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]