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8. New locus for autosomal dominant high myopia maps to the long arm of chromosome 17. Paluru P; Ronan SM; Heon E; Devoto M; Wildenberg SC; Scavello G; Holleschau A; Mäkitie O; Cole WG; King RA; Young TL Invest Ophthalmol Vis Sci; 2003 May; 44(5):1830-6. PubMed ID: 12714612 [TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26. Klein KM; Bromhead CJ; Smith KR; O'Callaghan CJ; Corcoran SJ; Heron SE; Iona X; Hodgson BL; McMahon JM; Lawrence KM; Scheffer IE; Dibbens LM; Bahlo M; Berkovic SF Neurology; 2013 Apr; 80(16):1485-93. PubMed ID: 23589636 [TBL] [Abstract][Full Text] [Related]
10. KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption. Assiry AA; Albalawi AM; Zafar MS; Khan SD; Ullah A; Almatrafi A; Ramzan K; Basit S Sci Rep; 2019 Nov; 9(1):16469. PubMed ID: 31712638 [TBL] [Abstract][Full Text] [Related]
11. An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29. Shugart YY; Silverberg MS; Duerr RH; Taylor KD; Wang MH; Zarfas K; Schumm LP; Bromfield G; Steinhart AH; Griffiths AM; Kane SV; Barmada MM; Rotter JI; Mei L; Bernstein CN; Bayless TM; Langelier D; Cohen A; Bitton A; Rioux JD; Cho JH; Brant SR Genes Immun; 2008 Mar; 9(2):161-7. PubMed ID: 18246054 [TBL] [Abstract][Full Text] [Related]
12. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15. Morlé L; Bozon M; Zech JC; Alloisio N; Raas-Rothschild A; Philippe C; Lambert JC; Godet J; Plauchu H; Edery P Am J Hum Genet; 2000 Dec; 67(6):1592-7. PubMed ID: 11035633 [TBL] [Abstract][Full Text] [Related]
13. Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23. Xu J; Zheng SL; Hawkins GA; Faith DA; Kelly B; Isaacs SD; Wiley KE; Chang B; Ewing CM; Bujnovszky P; Carpten JD; Bleecker ER; Walsh PC; Trent JM; Meyers DA; Isaacs WB Am J Hum Genet; 2001 Aug; 69(2):341-50. PubMed ID: 11443539 [TBL] [Abstract][Full Text] [Related]
14. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197 [TBL] [Abstract][Full Text] [Related]
15. Establishing the diagnostic criteria for eruption disorders based on genetic and clinical data. Rhoads SG; Hendricks HM; Frazier-Bowers SA Am J Orthod Dentofacial Orthop; 2013 Aug; 144(2):194-202. PubMed ID: 23910200 [TBL] [Abstract][Full Text] [Related]
16. A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1. Hmani-Aifa M; Ben Salem S; Benzina Z; Bouassida W; Messaoud R; Turki K; Khairallah M; Rebaï A; Fakhfekh F; Söderkvist P; Ayadi H Hum Genet; 2009 Oct; 126(4):575-87. PubMed ID: 19526372 [TBL] [Abstract][Full Text] [Related]
17. Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity. Braig DU; Schäffer AA; Glocker E; Salzer U; Warnatz K; Peter HH; Grimbacher B Hum Genet; 2003 Apr; 112(4):369-78. PubMed ID: 12574940 [TBL] [Abstract][Full Text] [Related]
18. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p. Chen S; Ondo WG; Rao S; Li L; Chen Q; Wang Q Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200 [TBL] [Abstract][Full Text] [Related]
19. A three-dimensional analysis of primary failure of eruption in humans and mice. Tokavanich N; Gupta A; Nagata M; Takahashi A; Matsushita Y; Yatabe M; Ruellas A; Cevidanes L; Maki K; Yamaguchi T; Ono N; Ono W Oral Dis; 2020 Mar; 26(2):391-400. PubMed ID: 31802584 [TBL] [Abstract][Full Text] [Related]
20. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families. Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]