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3. Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16. Watson ML; Wright AF; Macnicol AM; Allan PL; Clayton JF; Dempster M; Jeremiah SJ; Corney G; Hopkinson DA J Med Genet; 1987 Aug; 24(8):457-61. PubMed ID: 2821260 [TBL] [Abstract][Full Text] [Related]
4. Batten disease (Spielmeyer-Sjøgren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16. Eiberg H; Gardiner RM; Mohr J Clin Genet; 1989 Oct; 36(4):217-8. PubMed ID: 2805379 [TBL] [Abstract][Full Text] [Related]
5. Classification of hereditary cataracts in children by linkage analysis. Maumenee IH Ophthalmology; 1979 Sep; 86(9):1554-8. PubMed ID: 121767 [TBL] [Abstract][Full Text] [Related]
6. Close linkage between panic disorder and alpha-haptoglobin excluded in 10 families. Crowe RR; Noyes R; Samuelson S; Wesner R; Wilson R Arch Gen Psychiatry; 1990 Apr; 47(4):377-80. PubMed ID: 2322088 [TBL] [Abstract][Full Text] [Related]
8. A locus for isolated cataract on human Xp. Francis PJ; Berry V; Hardcastle AJ; Maher ER; Moore AT; Bhattacharya SS J Med Genet; 2002 Feb; 39(2):105-9. PubMed ID: 11836358 [TBL] [Abstract][Full Text] [Related]
9. Tyrosine aminotransferase and chymotrypsinogen B are linked to haptoglobin on human chromosome 16q: comparison of genetic and physical distances. Westphal EM; Burmeister M; Wienker TF; Lehrach H; Bender K; Scherer G Genomics; 1987 Dec; 1(4):313-9. PubMed ID: 2896626 [TBL] [Abstract][Full Text] [Related]
10. A locus for autosomal dominant anterior polar cataract on chromosome 17p. Berry V; Ionides AC; Moore AT; Plant C; Bhattacharya SS; Shiels A Hum Mol Genet; 1996 Mar; 5(3):415-9. PubMed ID: 8852669 [TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant zonular cataract with sutural opacities in a four-generation family. Basti S; Hejtmancik JF; Padma T; Ayyagari R; Kaiser-Kupfer MI; Murty JS; Rao GN Am J Ophthalmol; 1996 Feb; 121(2):162-8. PubMed ID: 8623885 [TBL] [Abstract][Full Text] [Related]
12. Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Eiberg H; Lund AM; Warburg M; Rosenberg T Hum Genet; 1995 Jul; 96(1):33-8. PubMed ID: 7607651 [TBL] [Abstract][Full Text] [Related]
13. Linkage analysis and the inheritance of arches in a Habbanite isolate. Anderson MW; Bonné-Tamir B; Carmelli D; Thompson EA Am J Hum Genet; 1979 Sep; 31(5):620-9. PubMed ID: 292307 [TBL] [Abstract][Full Text] [Related]
14. Segregation and linkage analysis of a large kindred of unipolar depression. Crowe RR; Namboodiri KK; Ashby HB; Elston RC Neuropsychobiology; 1981; 7(1):20-5. PubMed ID: 6936612 [TBL] [Abstract][Full Text] [Related]
15. Genetic linkage map of 46 DNA markers on human chromosome 16. Keith TP; Green P; Reeders ST; Brown VA; Phipps P; Bricker A; Falls K; Rediker KS; Powers JA; Hogan C Proc Natl Acad Sci U S A; 1990 Aug; 87(15):5754-8. PubMed ID: 2377614 [TBL] [Abstract][Full Text] [Related]
17. Linkage relations of a locus for congenital total nuclear cataract. Huntzinger RS; Weitkamp LR; Roca PD J Med Genet; 1978 Apr; 15(2):113-5. PubMed ID: 305964 [TBL] [Abstract][Full Text] [Related]
18. Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion region. Kidd KK; Kidd JR; Castiglione CM; Pakstis AJ; Sparkes RS Genet Epidemiol; 1986; 3(3):195-200. PubMed ID: 2873080 [TBL] [Abstract][Full Text] [Related]
19. Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35. Rogaev EI; Rogaeva EA; Korovaitseva GI; Farrer LA; Petrin AN; Keryanov SA; Turaeva S; Chumakov I; St George-Hyslop P; Ginter EK Hum Mol Genet; 1996 May; 5(5):699-703. PubMed ID: 8733140 [TBL] [Abstract][Full Text] [Related]
20. [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] [Next] [New Search]