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Items: 1 to 20 of 131

1.

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
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.

[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
4.

Familial Scheuermann disease: a genetic and linkage study.

McKenzie L, Sillence D.

J Med Genet. 1992 Jan;29(1):41-5.

5.

Dominant inheritance of Scheuermann's juvenile kyphosis.

Halal F, Gledhill RB, Fraser C.

Am J Dis Child. 1978 Nov;132(11):1105-7.

PMID:
717319
6.

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
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.

[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
9.

Familial lumbar Scheuermann disease with idiopathic scoliosis in China: First case report.

Dai Y, Li Y, Li P, Li L, Tu Z, Wang B.

Medicine (Baltimore). 2017 Jun;96(25):e7100. doi: 10.1097/MD.0000000000007100.

10.

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.

Chu K, Koller DL, Snyder R, Fishburn T, Lai D, Waguespack SG, Foroud T, Econs MJ.

Bone. 2005 Nov;37(5):655-61. Epub 2005 Aug 24.

PMID:
16120485
11.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
12.

Segregation analysis of microcephaly.

Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A.

Am J Med Genet. 1996 Oct 28;65(3):226-34.

PMID:
9240749
13.

Identification of candidate regions for familial idiopathic scoliosis.

Miller NH, Justice CM, Marosy B, Doheny KF, Pugh E, Zhang J, Dietz HC 3rd, Wilson AF.

Spine (Phila Pa 1976). 2005 May 15;30(10):1181-7.

PMID:
15897833
14.

Lack of association between the aggrecan gene and familial idiopathic scoliosis.

Marosy B, Justice CM, Nzegwu N, Kumar G, Wilson AF, Miller NH.

Spine (Phila Pa 1976). 2006 Jun 1;31(13):1420-5.

PMID:
16741449
15.

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 22;104(2):120-6.

PMID:
11746041
16.

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?

Ma S, Davis TL, Blair MA, Fang JY, Bradford Y, Haines JL, Hedera P.

Mov Disord. 2006 Sep;21(9):1368-74.

PMID:
16721753
17.

The search for idiopathic scoliosis genes.

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

Spine (Phila Pa 1976). 2006 Mar 15;31(6):679-81.

PMID:
16540873
18.

A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.

Jimenez-Escrig A, Gomez-Tortosa E, Baron M, Rabano A, Arcos-Burgos M, Palacios LG, Yusta A, Anta P, Perez I, Hierro M, Munoz DG, Barquero S.

Brain. 2005 Jul;128(Pt 7):1707-15. Epub 2005 Apr 20.

PMID:
15843424
19.

Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees.

Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC.

Eur J Hum Genet. 2002 Jun;10(6):367-74.

20.

Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.

Morcuende JA, Minhas R, Dolan L, Stevens J, Beck J, Wang K, Weinstein SL, Sheffield V.

Spine (Phila Pa 1976). 2003 Sep 1;28(17):2025-8; discussion 2029.

PMID:
12973153

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