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Results: 1 to 20 of 91

Similar articles for PubMed (Select 1415339)

1.

Oculoauriculovertebral anomaly: segregation analysis.

Kaye CI, Martin AO, Rollnick BR, Nagatoshi K, Israel J, Hermanoff M, Tropea B, Richtsmeier JT, Morton NE.

Am J Med Genet. 1992 Aug 1;43(6):913-7.

PMID:
1415339
2.

Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature.

Vendramini-Pittoli S, Kokitsu-Nakata NM.

Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Review.

PMID:
19305190
3.

A family with dominant oculoauriculovertebral spectrum.

Stoll C, Viville B, Treisser A, Gasser B.

Am J Med Genet. 1998 Jul 24;78(4):345-9.

PMID:
9714437
4.

Segregation analysis of NIDDM in Caucasian families.

Cook JT, Shields DC, Page RC, Levy JC, Hattersley AT, Shaw JA, Neil HA, Wainscoat JS, Turner RC.

Diabetologia. 1994 Dec;37(12):1231-40.

PMID:
7895953
5.

Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism.

Ritvo ER, Spence MA, Freeman BJ, Mason-Brothers A, Mo A, Marazita ML.

Am J Psychiatry. 1985 Feb;142(2):187-92.

PMID:
4038589
6.

A family with autosomal dominant oculo-auriculo-vertebral spectrum.

Tasse C, Majewski F, Böhringer S, Fischer S, Lüdecke HJ, Gillessen-Kaesbach G, Wieczorek D.

Clin Dysmorphol. 2007 Jan;16(1):1-7. Review.

PMID:
17159507
7.

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.

8.

Inheritance of astigmatism: evidence for a major autosomal dominant locus.

Clementi M, Angi M, Forabosco P, Di Gianantonio E, Tenconi R.

Am J Hum Genet. 1998 Sep;63(3):825-30.

9.

Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients.

Rollnick BR, Kaye CI, Nagatoshi K, Hauck W, Martin AO.

Am J Med Genet. 1987 Feb;26(2):361-75.

PMID:
3812588
10.

Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia.

Regenbogen L, Godel V, Goya V, Goodman RM.

Clin Genet. 1982 Mar;21(3):161-7. No abstract available.

PMID:
7094392
11.

Hemifacial microsomia and variants: pedigree data.

Rollnick BR, Kaye CI.

Am J Med Genet. 1983 Jun;15(2):233-53.

PMID:
6881197
12.

Familial hemifacial microsomia due to autosomal dominant inheritance. Case reports.

Singer SL, Haan E, Slee J, Goldblatt J.

Aust Dent J. 1994 Oct;39(5):287-91.

PMID:
7811205
13.

Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results.

Ottman R, Hauser WA, Barker-Cummings C, Lee JH, Risch N.

Am J Hum Genet. 1997 Mar;60(3):667-75.

14.

Segregation analysis of Alagille syndrome.

Dhorne-Pollet S, Deleuze JF, Hadchouel M, Bonaïti-Pellié C.

J Med Genet. 1994 Jun;31(6):453-7.

15.

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
16.

Genetic analysis of cleft lip with or without cleft palate in Danish kindreds.

Marazita ML, Spence MA, Melnick M.

Am J Med Genet. 1984 Sep;19(1):9-18.

PMID:
6496575
17.

Segregation analysis of 231 Ashkenazi Jewish families for evidence of additional breast cancer susceptibility genes.

Kaufman DJ, Beaty TH, Struewing JP.

Cancer Epidemiol Biomarkers Prev. 2003 Oct;12(10):1045-52.

18.

Genetic segregation analysis of recurrent, early-onset major depression: evidence for single major locus transmission.

Maher BS, Marazita ML, Zubenko WN, Spiker DG, Giles DE, Kaplan BB, Zubenko GS.

Am J Med Genet. 2002 Mar 8;114(2):214-21.

PMID:
11857584
19.

Commingling and segregation analysis of reading performance in families of normal reading probands.

Gilger JW, Borecki IB, DeFries JC, Pennington BF.

Behav Genet. 1994 Jul;24(4):345-55.

PMID:
7993313
20.

31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.

Engiz O, Balci S, Unsal M, Ozer S, Oguz KK, Aktas D.

Genet Couns. 2007;18(3):277-88.

PMID:
18019368
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