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22. 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]
23. Homozygosity mapping of the locus responsible for renal tubular dysplasia of cattle on bovine chromosome 1. Ohba Y; Kitagawa H; Kitoh K; Asahina S; Nishimori K; Yoneda K; Kunieda T; Sasaki Y Mamm Genome; 2000 Apr; 11(4):316-9. PubMed ID: 10754108 [TBL] [Abstract][Full Text] [Related]
24. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. Tsujikawa M; Kurahashi H; Tanaka T; Okada M; Yamamoto S; Maeda N; Watanabe H; Inoue Y; Kiridoshi A; Matsumoto K; Ohashi Y; Kinoshita S; Shimomura Y; Nakamura Y; Tano Y Am J Hum Genet; 1998 Oct; 63(4):1073-7. PubMed ID: 9758629 [TBL] [Abstract][Full Text] [Related]
25. Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19. Oehlmann R; Summerville GP; Yeh G; Weaver EJ; Jimenez SA; Knowlton RG Am J Hum Genet; 1994 Jan; 54(1):3-10. PubMed ID: 8279467 [TBL] [Abstract][Full Text] [Related]
26. DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12. Wajid M; Abbasi AA; Ansar M; Pham TL; Yan K; Haque S; Ahmad W; Leal SM Eur J Hum Genet; 2003 Oct; 11(10):812-5. PubMed ID: 14512973 [TBL] [Abstract][Full Text] [Related]
27. Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43. Parvari R; Hershkovitz E; Kanis A; Gorodischer R; Shalitin S; Sheffield VC; Carmi R Am J Hum Genet; 1998 Jul; 63(1):163-9. PubMed ID: 9634513 [TBL] [Abstract][Full Text] [Related]
28. Homozygosity mapping of Portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity. Moreira MC; Barbot C; Tachi N; Kozuka N; Mendonça P; Barros J; Coutinho P; Sequeiros J; Koenig M Am J Hum Genet; 2001 Feb; 68(2):501-8. PubMed ID: 11170899 [TBL] [Abstract][Full Text] [Related]
29. Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community. Farrer LA; Bowirrat A; Friedland RP; Waraska K; Korczyn AD; Baldwin CT Hum Mol Genet; 2003 Feb; 12(4):415-22. PubMed ID: 12566388 [TBL] [Abstract][Full Text] [Related]
30. The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27. Leegwater PA; Könst AA; Kuyt B; Sandkuijl LA; Naidu S; Oudejans CB; Schutgens RB; Pronk JC; van der Knaap MS Am J Hum Genet; 1999 Sep; 65(3):728-34. PubMed ID: 10441579 [TBL] [Abstract][Full Text] [Related]
31. Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint. Walder RY; Shalev H; Brennan TM; Carmi R; Elbedour K; Scott DA; Hanauer A; Mark AL; Patil S; Stone EM; Sheffield VC Hum Mol Genet; 1997 Sep; 6(9):1491-7. PubMed ID: 9285786 [TBL] [Abstract][Full Text] [Related]
32. High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene. Sulisalo T; Klockars J; Mäkitie O; Francomano CA; de la Chapelle A; Kaitila I; Sistonen P Am J Hum Genet; 1994 Nov; 55(5):937-45. PubMed ID: 7977356 [TBL] [Abstract][Full Text] [Related]
33. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping. Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098 [TBL] [Abstract][Full Text] [Related]
34. Giant axonal neuropathy locus refinement to a < 590 kb critical interval. Cavalier L; BenHamida C; Amouri R; Belal S; Bomont P; Lagarde N; Gressin L; Callen D; Demir E; Topaloglu H; Landrieu P; Ioos C; Hamida MB; Koenig M; Hentati F Eur J Hum Genet; 2000 Jul; 8(7):527-34. PubMed ID: 10909853 [TBL] [Abstract][Full Text] [Related]
36. Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling. Arbour NC; Zlotogora J; Knowlton RG; Merin S; Rosenmann A; Kanis AB; Rokhlina T; Stone EM; Sheffield VC Hum Mol Genet; 1997 May; 6(5):689-94. PubMed ID: 9158143 [TBL] [Abstract][Full Text] [Related]
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38. Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression. Coon H; Hoff M; Holik J; Hadley D; Fang N; Reimherr F; Wender P; Byerley W Biol Psychiatry; 1996 Apr; 39(8):689-96. PubMed ID: 8731455 [TBL] [Abstract][Full Text] [Related]
39. Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia. Bernard LE; Chitayat D; Weksberg R; Van Allen MI; Langlois S J Med Genet; 1996 May; 33(5):432-4. PubMed ID: 8733060 [TBL] [Abstract][Full Text] [Related]
40. A gene for Meckel syndrome maps to chromosome 11q13. Roume J; Genin E; Cormier-Daire V; Ma HW; Mehaye B; Attie T; Razavi-Encha F; Fallet-Bianco C; Buenerd A; Clerget-Darpoux F; Munnich A; Le Merrer M Am J Hum Genet; 1998 Oct; 63(4):1095-101. PubMed ID: 9758620 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]