458 related articles for article (PubMed ID: 15759859)
21. Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
Paluru PC; Nallasamy S; Devoto M; Rappaport EF; Young TL
Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2300-7. PubMed ID: 15980214
[TBL] [Abstract][Full Text] [Related]
22. Autosomal recessive inheritance of myopia in Hong Kong Chinese infants.
Edwards M; Lewis WH
Ophthalmic Physiol Opt; 1991 Jul; 11(3):227-31. PubMed ID: 1766686
[TBL] [Abstract][Full Text] [Related]
23. Complex segregation analysis of obsessive-compulsive disorder in families with pediatric probands.
Hanna GL; Fingerlin TE; Himle JA; Boehnke M
Hum Hered; 2005; 60(1):1-9. PubMed ID: 16088199
[TBL] [Abstract][Full Text] [Related]
24. [The inheritance of hypodontia in families--the segregational analysis].
Jursić A; Skrinjarić I
Acta Stomatol Croat; 1988; 22(4):261-9. PubMed ID: 3255247
[TBL] [Abstract][Full Text] [Related]
25. Segregation analysis of smoking-associated malignancies: evidence for Mendelian inheritance.
Sellers TA; Chen PL; Potter JD; Bailey-Wilson JE; Rothschild H; Elston RC
Am J Med Genet; 1994 Sep; 52(3):308-14. PubMed ID: 7810562
[TBL] [Abstract][Full Text] [Related]
26. [Linkage analysis of one family with autosomal dominant high myopia].
Chang JX; Zhang DD; Lin Y; Liu B; Lu F; Tang X; Yang Y; Chen B; Zhang CJ; Yang ZL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):424-6. PubMed ID: 18683142
[TBL] [Abstract][Full Text] [Related]
27. Segregation analysis suggests that keratoconus is a complex non-mendelian disease.
Kriszt A; Losonczy G; Berta A; Vereb G; Takács L
Acta Ophthalmol; 2014 Nov; 92(7):e562-8. PubMed ID: 24629050
[TBL] [Abstract][Full Text] [Related]
28. A genome-wide scan maps a novel high myopia locus to 5p15.
Lam CY; Tam PO; Fan DS; Fan BJ; Wang DY; Lee CW; Pang CP; Lam DS
Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):3768-78. PubMed ID: 18421076
[TBL] [Abstract][Full Text] [Related]
29. Family study of the inheritance of pectus excavatum.
Creswick HA; Stacey MW; Kelly RE; Gustin T; Nuss D; Harvey H; Goretsky MJ; Vasser E; Welch JC; Mitchell K; Proud VK
J Pediatr Surg; 2006 Oct; 41(10):1699-703. PubMed ID: 17011272
[TBL] [Abstract][Full Text] [Related]
30. Genetic epidemiology of glioma.
Malmer B; Iselius L; Holmberg E; Collins A; Henriksson R; Grönberg H
Br J Cancer; 2001 Feb; 84(3):429-34. PubMed ID: 11161412
[TBL] [Abstract][Full Text] [Related]
31. Segregation ratio in cranio-cerebello-cardiac syndrome.
Stellingwerff HJ; van Hagen JM; ten Kate LP
Eur J Hum Genet; 2006 Sep; 14(9):1054-7. PubMed ID: 16736035
[TBL] [Abstract][Full Text] [Related]
32. [Study of 315 pedigrees with idiopathic mental retardation by segregation analysis].
Hu Y
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1992 Jun; 25(3):157-9, 191. PubMed ID: 1395944
[TBL] [Abstract][Full Text] [Related]
33. [Planning selection for informativity of linkage analysis of separate pedigrees].
Aksenovich TI; Ginzburg EKh
Genetika; 1993 Aug; 29(8):1394-403. PubMed ID: 8405980
[TBL] [Abstract][Full Text] [Related]
34. [Medico-genetical study of the population of the Kostroma Region. IV. Genetic load and diversity of hereditary pathology in 5 districts].
Petrin AN; Ginter EK; Rudenskaia GE; Burkova LM; Khlebnikova OV
Genetika; 1987 Jul; 23(7):1319-27. PubMed ID: 2958387
[TBL] [Abstract][Full Text] [Related]
35. Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
Passos-Bueno MR; Marie SK; Monteiro M; Neustein I; Whittle MR; Vainzof M; Zatz M
Am J Med Genet; 1994 Aug; 52(2):170-3. PubMed ID: 7802003
[TBL] [Abstract][Full Text] [Related]
36. Power of segregation analysis for detection of major gene effects on quantitative traits.
Borecki IB; Province MA; Rao DC
Genet Epidemiol; 1994; 11(5):409-18. PubMed ID: 7835687
[TBL] [Abstract][Full Text] [Related]
37. Segregation analysis of cutaneous melanoma in Queensland.
Aitken JF; Bailey-Wilson J; Green AC; MacLennan R; Martin NG
Genet Epidemiol; 1998; 15(4):391-401. PubMed ID: 9671988
[TBL] [Abstract][Full Text] [Related]
38. Genome-wide scan for myopia in the Old Order Amish.
Stambolian D; Ciner EB; Reider LC; Moy C; Dana D; Owens R; Schlifka M; Holmes T; Ibay G; Bailey-Wilson JE
Am J Ophthalmol; 2005 Sep; 140(3):469-76. PubMed ID: 16084785
[TBL] [Abstract][Full Text] [Related]
39. Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.
Martinez M; Campion D; Babron MC; Hannequin D; Agid Y; Bellis M; Brice A; Mallet J; Michon A; Thomas-Anterion C; Clerget-Darpoux F
Am J Med Genet; 1996 Feb; 67(1):9-12. PubMed ID: 8678122
[TBL] [Abstract][Full Text] [Related]
40. Segregation analysis of leprosy in families of northern Thailand.
Wagener DK; Schauf V; Nelson KE; Scollard D; Brown A; Smith T
Genet Epidemiol; 1988; 5(2):95-105. PubMed ID: 3402727
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]