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.
132 related articles for article (PubMed ID: 8554065)
21. Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec. De Braekeleer M; Dallaire A; Mathieu J Hum Genet; 1993 Apr; 91(3):223-7. PubMed ID: 8386695 [TBL] [Abstract][Full Text] [Related]
22. Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families. Watts GD; O'Briant KC; Chance PF Hum Genet; 2002 Feb; 110(2):166-72. PubMed ID: 11935323 [TBL] [Abstract][Full Text] [Related]
23. A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3. Bouhouche A; Benomar A; Birouk N; Mularoni A; Meggouh F; Tassin J; Grid D; Vandenberghe A; Yahyaoui M; Chkili T; Brice A; LeGuern E Am J Hum Genet; 1999 Sep; 65(3):722-7. PubMed ID: 10441578 [TBL] [Abstract][Full Text] [Related]
24. Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population. Rivard SR; Lanzara C; Grimard D; Carella M; Simard H; Ficarella R; Simard R; D'Adamo AP; Férec C; Camaschella C; Mura C; Roetto A; De Braekeleer M; Bechner L; Gasparini P Eur J Hum Genet; 2003 Aug; 11(8):585-9. PubMed ID: 12891378 [TBL] [Abstract][Full Text] [Related]
25. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum. França MC; D'Abreu A; Maurer-Morelli CV; Seccolin R; Appenzeller S; Alessio A; Damasceno BP; Nucci A; Cendes F; Lopes-Cendes I Mov Disord; 2007 Aug; 22(11):1556-62. PubMed ID: 17516453 [TBL] [Abstract][Full Text] [Related]
26. The Andermann syndrome: agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy. Larbrisseau A; Vanasse M; Brochu P; Jasmin G Can J Neurol Sci; 1984 May; 11(2):257-61. PubMed ID: 6329500 [TBL] [Abstract][Full Text] [Related]
27. Agenesis of the corpus callosum associated with MASA syndrome. Boyd E; Schwartz CE; Schroer RJ; May MM; Shapiro SD; Arena JF; Lubs HA; Stevenson RE Clin Dysmorphol; 1993 Oct; 2(4):332-41. PubMed ID: 8305964 [TBL] [Abstract][Full Text] [Related]
28. The acrocallosal syndrome and Greig syndrome are not allelic disorders. Brueton LA; Chotai KA; van Herwerden L; Schinzel A; Winter RM J Med Genet; 1992 Sep; 29(9):635-7. PubMed ID: 1404293 [TBL] [Abstract][Full Text] [Related]
29. Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1. Mariman EC; Gabreëls-Festen AA; van Beersum SE; Jongen PJ; Ropers HH; Gabreëls FJ Hum Genet; 1993 Aug; 92(1):87-90. PubMed ID: 8396068 [TBL] [Abstract][Full Text] [Related]
30. Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypes. Slaugenhaupt SA; Acierno JS; Helbling LA; Bove C; Goldin E; Bach G; Schiffmann R; Gusella JF Am J Hum Genet; 1999 Sep; 65(3):773-8. PubMed ID: 10441585 [TBL] [Abstract][Full Text] [Related]
32. The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q. Kibar Z; Der Kaloustian VM; Brais B; Hani V; Fraser FC; Rouleau GA Hum Mol Genet; 1996 Apr; 5(4):543-7. PubMed ID: 8845850 [TBL] [Abstract][Full Text] [Related]
33. Chorea-acanthocytosis: genetic linkage to chromosome 9q21. Rubio JP; Danek A; Stone C; Chalmers R; Wood N; Verellen C; Ferrer X; Malandrini A; Fabrizi GM; Manfredi M; Vance J; Pericak-Vance M; Brown R; Rudolf G; Picard F; Alonso E; Brin M; Németh AH; Farrall M; Monaco AP Am J Hum Genet; 1997 Oct; 61(4):899-908. PubMed ID: 9382101 [TBL] [Abstract][Full Text] [Related]
34. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15. Stöber G; Saar K; Rüschendorf F; Meyer J; Nürnberg G; Jatzke S; Franzek E; Reis A; Lesch KP; Wienker TF; Beckmann H Am J Hum Genet; 2000 Nov; 67(5):1201-7. PubMed ID: 11001582 [TBL] [Abstract][Full Text] [Related]
35. The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q. Serratosa JM; Delgado-Escueta AV; Posada I; Shih S; Drury I; Berciano J; Zabala JA; Antúnez MC; Sparkes RS Hum Mol Genet; 1995 Sep; 4(9):1657-63. PubMed ID: 8541857 [TBL] [Abstract][Full Text] [Related]
36. Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder. Meyer J; Johannssen K; Freitag CM; Schraut K; Teuber I; Hahner A; Mainhardt C; Mössner R; Volz HP; Wienker TF; McKeane D; Stephan DA; Rouleau G; Reif A; Lesch KP Int J Neuropsychopharmacol; 2005 Dec; 8(4):495-504. PubMed ID: 16098236 [TBL] [Abstract][Full Text] [Related]
37. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search. Gasparini P; Miraglia del Giudice E; Delaunay J; Totaro A; Granatiero M; Melchionda S; Zelante L; Iolascon A Am J Hum Genet; 1997 Nov; 61(5):1112-6. PubMed ID: 9345103 [TBL] [Abstract][Full Text] [Related]
38. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26. McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837 [TBL] [Abstract][Full Text] [Related]
39. A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1q. Jackson SN; Pinkney J; Bargiotta A; Veal CD; Howlett TA; McNally PG; Corral R; Johnson A; Trembath RC Am J Hum Genet; 1998 Aug; 63(2):534-40. PubMed ID: 9683602 [TBL] [Abstract][Full Text] [Related]