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Items: 1 to 20 of 153

1.

[New models of inheritance of complex characteristics and their use in segregation analysis of idiopathic scoliosis].

Aksenovich TI, Zaĭdman AM, Zorkol'tseva IV, Tregubova IL, Borodin PM.

Genetika. 1999 Feb;35(2):255-62. Russian.

PMID:
10495942
2.

Segregation analysis of idiopathic scoliosis: demonstration of a major gene effect.

Axenovich TI, Zaidman AM, Zorkoltseva IV, Tregubova IL, Borodin PM.

Am J Med Genet. 1999 Oct 8;86(4):389-94.

PMID:
10494097
3.

Segregation analysis of Scheuermann disease in ninety families from Siberia.

Axenovich TI, Zaidman AM, Zorkoltseva IV, Kalashnikova EV, Borodin PM.

Am J Med Genet. 2001 May 15;100(4):275-9.

PMID:
11343318
4.

[Genetics of idiopathic scoliosis].

Bonaïti C, Feingold J, Briard ML, Lapeyre F, Rigault P, Guivarch J.

Helv Paediatr Acta. 1976 Oct;31(3):229-40. French.

PMID:
977374
5.

Polygenic inheritance of adolescent idiopathic scoliosis: a study of extended families in Utah.

Ward K, Ogilvie J, Argyle V, Nelson L, Meade M, Braun J, Chettier R.

Am J Med Genet A. 2010 May;152A(5):1178-88. doi: 10.1002/ajmg.a.33145.

PMID:
20425822
6.

Familial segregation of venous thromboembolism.

Heit JA, Phelps MA, Ward SA, Slusser JP, Petterson TM, De Andrade M.

J Thromb Haemost. 2004 May;2(5):731-6.

7.

Segregation analysis of prostate cancer in France: evidence for autosomal dominant inheritance and residual brother-brother dependence.

Valeri A, Briollais L, Azzouzi R, Fournier G, Mangin P, Berthon P, Cussenot O, Demenais F.

Ann Hum Genet. 2003 Mar;67(Pt 2):125-37.

PMID:
12675688
8.

[Preliminary analysis of inheritance of scoliosis].

Aksenovich TI, Semenov IR, Ginzburg EKh, Zaĭdman AM.

Genetika. 1988 Nov;24(11):2056-63. Russian.

PMID:
3234750
9.

Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.

Justice CM, Miller NH, Marosy B, Zhang J, Wilson AF.

Spine (Phila Pa 1976). 2003 Mar 15;28(6):589-94.

PMID:
12642767
10.

[Analysis of polymorphism of the number of tandem repeats in the aggrecan gene exon G3 in the families with idiopathic scoliosis].

Zorkol'tseva IV, Liubinskiĭ OA, Sharipov RN, Zaĭdman AM, Aksenovich TI, Dymshits GM.

Genetika. 2002 Feb;38(2):259-63. Russian.

PMID:
11898616
11.

Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China.

Zhang W, Bailey-Wilson JE, Li W, Wang X, Zhang C, Mao X, Liu Z, Zhou C, Wu M.

Am J Hum Genet. 2000 Jul;67(1):110-9. Epub 2000 Jun 6.

12.

Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.

Risch NJ, Bressman SB, deLeon D, Brin MF, Burke RE, Greene PE, Shale H, Claus EB, Cupples LA, Fahn S.

Am J Hum Genet. 1990 Mar;46(3):533-8.

13.

Major gene and multifactorial inheritance of mandibular prognathism.

Cruz RM, Krieger H, Ferreira R, Mah J, Hartsfield J Jr, Oliveira S.

Am J Med Genet A. 2008 Jan 1;146A(1):71-7.

PMID:
18074368
14.

Positional cloning strategies for idiopathic scoliosis.

Bashiardes S, Veile R, Wise CA, Szappanos L, Lovett M.

Stud Health Technol Inform. 2002;91:86-9.

PMID:
15457700
15.

Segregation of structural collagen genes in adolescent idiopathic scoliosis.

Carr AJ, Ogilvie DJ, Wordsworth BP, Priestly LM, Smith R, Sykes B.

Clin Orthop Relat Res. 1992 Jan;(274):305-10.

PMID:
1345899
16.

Major gene segregation of actinic prurigo among North American Indians in Saskatchewan.

Schnell AH, Elston RC, Hull PR, Lane PR.

Am J Med Genet. 2000 May 29;92(3):212-9.

PMID:
10817657
17.

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 16;67(1):9-12.

PMID:
8678122
18.

[Genetic aspect of dysplastic (idiopathic) scoliosis].

Levaia NV.

Ortop Travmatol Protez. 1981 Feb;(2):23-9. Russian. No abstract available.

PMID:
7015224
19.

Genetics of adolescent idiopathic scoliosis.

Czeizel A, Bellyei A, Barta O, Magda T, Molnár L.

J Med Genet. 1978 Dec;15(6):424-7.

20.

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