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Results: 10

1.

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC.

N Engl J Med. 2004 Aug 19;351(8):769-80.

PMID:
15317890
[PubMed - indexed for MEDLINE]
Free Article
2.

Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate.

Pezzetti F, Martinelli M, Scapoli L, Carinci F, Palmieri A, Marchesini J, Carinci P, Caramelli E, Rullo R, Gombos F, Tognon M.

Hum Mutat. 2004 Jul;24(1):104-5.

PMID:
15221800
[PubMed - indexed for MEDLINE]
3.

Cleft palate: players, pathways, and pursuits.

Murray JC, Schutte BC.

J Clin Invest. 2004 Jun;113(12):1676-8.

PMID:
15199400
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Pedigree disequilibrium tests for multilocus haplotypes.

Dudbridge F.

Genet Epidemiol. 2003 Sep;25(2):115-21.

PMID:
12916020
[PubMed - indexed for MEDLINE]
5.

Recent developments in orofacial cleft genetics.

Carinci F, Pezzetti F, Scapoli L, Martinelli M, Avantaggiato A, Carinci P, Padula E, Baciliero U, Gombos F, Laino G, Rullo R, Cenzi R, Carls F, Tognon M.

J Craniofac Surg. 2003 Mar;14(2):130-43. Review.

PMID:
12621282
[PubMed - indexed for MEDLINE]
6.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC.

Nat Genet. 2002 Oct;32(2):285-9. Epub 2002 Sep 3.

PMID:
12219090
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia.

Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA.

Nat Genet. 2000 Aug;25(4):427-30.

PMID:
10932188
[PubMed - indexed for MEDLINE]
8.

GOLD--graphical overview of linkage disequilibrium.

Abecasis GR, Cookson WO.

Bioinformatics. 2000 Feb;16(2):182-3.

PMID:
10842743
[PubMed - indexed for MEDLINE]
Free Article
9.

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.

Celli J, Duijf P, Hamel BC, Bamshad M, Kramer B, Smits AP, Newbury-Ecob R, Hennekam RC, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H.

Cell. 1999 Oct 15;99(2):143-53.

PMID:
10535733
[PubMed - indexed for MEDLINE]
Free Article
10.

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Spielman RS, McGinnis RE, Ewens WJ.

Am J Hum Genet. 1993 Mar;52(3):506-16.

PMID:
8447318
[PubMed - indexed for MEDLINE]
Free PMC Article

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