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.
112 related articles for article (PubMed ID: 21637415)
41. TetraploidMap for Windows: linkage map construction and QTL mapping in autotetraploid species. Hackett CA; Milne I; Bradshaw JE; Luo Z J Hered; 2007; 98(7):727-9. PubMed ID: 17965198 [TBL] [Abstract][Full Text] [Related]
42. Pseudo-likelihood estimates of the cumulative risk of an autosomal dominant disease from a kin-cohort study. Moore DF; Chatterjee N; Pee D; Gail MH Genet Epidemiol; 2001 Feb; 20(2):210-27. PubMed ID: 11180447 [TBL] [Abstract][Full Text] [Related]
43. Genetic counseling for autosomal dominant diseases with a negative family history. Friedman JM Clin Genet; 1985 Jan; 27(1):68-71. PubMed ID: 3978840 [TBL] [Abstract][Full Text] [Related]
44. PopABC: a program to infer historical demographic parameters. Lopes JS; Balding D; Beaumont MA Bioinformatics; 2009 Oct; 25(20):2747-9. PubMed ID: 19679678 [TBL] [Abstract][Full Text] [Related]
45. Estimation of penetrance from twin data. Praxedes LA; Otto PA Twin Res; 2000 Dec; 3(4):294-8. PubMed ID: 11463150 [TBL] [Abstract][Full Text] [Related]
46. Estimating ancestry and heterozygosity of hybrids using molecular markers. Fitzpatrick BM BMC Evol Biol; 2012 Jul; 12():131. PubMed ID: 22849298 [TBL] [Abstract][Full Text] [Related]
47. Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome. Barr CL; Best L; Weksberg R Am J Med Genet; 2001 Nov; 104(2):120-6. PubMed ID: 11746041 [TBL] [Abstract][Full Text] [Related]
48. Kinship testing with X-chromosomal markers: mathematical and statistical issues. Krawczak M Forensic Sci Int Genet; 2007 Jun; 1(2):111-4. PubMed ID: 19083739 [TBL] [Abstract][Full Text] [Related]
49. The relative efficiency of penetrance estimators for sib pairs. Swartz MD; Minard CG; Amos CI Hum Hered; 2005; 59(1):61-6. PubMed ID: 15855789 [TBL] [Abstract][Full Text] [Related]
50. Estimating the power of variance component linkage analysis in large pedigrees. Chen WM; Abecasis GR Genet Epidemiol; 2006 Sep; 30(6):471-84. PubMed ID: 16685720 [TBL] [Abstract][Full Text] [Related]
55. Complex segregation analysis of pedigrees from the Gilda Radner Familial Ovarian Cancer Registry reveals evidence for mendelian dominant inheritance. Tayo BO; DiCioccio RA; Liang Y; Trevisan M; Cooper RS; Lele S; Sucheston L; Piver SM; Odunsi K PLoS One; 2009 Jun; 4(6):e5939. PubMed ID: 19536330 [TBL] [Abstract][Full Text] [Related]
56. Familial clustering of medullary sponge kidney is autosomal dominant with reduced penetrance and variable expressivity. Fabris A; Lupo A; Ferraro PM; Anglani F; Pei Y; Danza FM; Gambaro G Kidney Int; 2013 Feb; 83(2):272-7. PubMed ID: 23223172 [TBL] [Abstract][Full Text] [Related]
57. Maximum-likelihood estimation of allelic dropout and false allele error rates from microsatellite genotypes in the absence of reference data. Johnson PC; Haydon DT Genetics; 2007 Feb; 175(2):827-42. PubMed ID: 17179070 [TBL] [Abstract][Full Text] [Related]
58. [Variations in expressivity and penetrance of hypodontia]. Jursić A; Skrinjarić I Acta Stomatol Croat; 1989; 23(1):13-8. PubMed ID: 2634917 [TBL] [Abstract][Full Text] [Related]
59. Friends and family: A software program for identification of unrelated individuals from molecular marker data. de Jager D; Swarts P; Harper C; Bloomer P Mol Ecol Resour; 2017 Nov; 17(6):e225-e233. PubMed ID: 28503747 [TBL] [Abstract][Full Text] [Related]
60. Experience with the Internet release of AIDA v4.0--http://www.diabetic.org.uk.aida.htm--an interactive educational diabetes simulator. Lehmann ED Diabetes Technol Ther; 1999; 1(1):41-54. PubMed ID: 11475304 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]