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.
3. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161 [TBL] [Abstract][Full Text] [Related]
4. [An attempt to locate the gene for congenital cataracts using linkage analysis]. Ginter EK; Petrin AN; Spitsyn VA; Rogaev EI Genetika; 1991 Oct; 27(10):1840-9. PubMed ID: 1778455 [TBL] [Abstract][Full Text] [Related]
5. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family. Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218 [TBL] [Abstract][Full Text] [Related]
6. Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract. Carter JM; McLean WH; West S; Quinlan RA Biochem Biophys Res Commun; 2000 Apr; 270(2):432-6. PubMed ID: 10753642 [TBL] [Abstract][Full Text] [Related]
7. The PITX3 gene in posterior polar congenital cataract in Australia. Burdon KP; McKay JD; Wirth MG; Russell-Eggit IM; Bhatti S; Ruddle JB; Dimasi D; Mackey DA; Craig JE Mol Vis; 2006 Apr; 12():367-71. PubMed ID: 16636655 [TBL] [Abstract][Full Text] [Related]
8. A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q. Mackay DS; Andley UP; Shiels A Mol Vis; 2004 Mar; 10():155-62. PubMed ID: 15041957 [TBL] [Abstract][Full Text] [Related]
9. A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract. Li Y; Wang J; Dong B; Man H Mol Vis; 2004 Sep; 10():668-71. PubMed ID: 15448617 [TBL] [Abstract][Full Text] [Related]
10. X-linked or autosomal dominant, lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? A reappraisal. Gorlin RJ; Knier J Am J Med Genet; 1982 Dec; 13(4):465-7. PubMed ID: 7158645 [No Abstract] [Full Text] [Related]
11. A new locus for autosomal dominant congenital cataracts maps to chromosome 3. Kramer PL; LaMorticella D; Schilling K; Billingslea AM; Weleber RG; Litt M Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):36-9. PubMed ID: 10634598 [TBL] [Abstract][Full Text] [Related]
12. A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. Addison PK; Berry V; Holden KR; Espinal D; Rivera B; Su H; Srivastava AK; Bhattacharya SS Mol Vis; 2006 Jul; 12():791-5. PubMed ID: 16885921 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A gene for autosomal dominant congenital nystagmus localizes to 6p12. Kerrison JB; Arnould VJ; Barmada MM; Koenekoop RK; Schmeckpeper BJ; Maumenee IH Genomics; 1996 May; 33(3):523-6. PubMed ID: 8661013 [TBL] [Abstract][Full Text] [Related]
16. A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family. Khaliq S; Hameed A; Ismail M; Anwar K; Mehdi SQ Invest Ophthalmol Vis Sci; 2002 Jul; 43(7):2083-7. PubMed ID: 12091400 [TBL] [Abstract][Full Text] [Related]
18. On the inheritance of primary spontaneous pneumothorax. Abolnik IZ; Lossos IS; Zlotogora J; Brauer R Am J Med Genet; 1991 Aug; 40(2):155-8. PubMed ID: 1897568 [TBL] [Abstract][Full Text] [Related]
19. A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes. Bateman JB; Richter L; Flodman P; Burch D; Brown S; Penrose P; Paul O; Geyer DD; Brooks DG; Spence MA Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3441-9. PubMed ID: 16877414 [TBL] [Abstract][Full Text] [Related]
20. Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts. Bodker FS; Lavery MA; Mitchell TN; Lovrien EW; Maumenee IH Am J Med Genet; 1990 Sep; 37(1):54-9. PubMed ID: 2240043 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]