Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations. - Wikidata - awgldk - TriplyDB

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

http://www.wikidata.org/entity/Q33740394

about

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate Genomic expression in non syndromic cleft lip and palate patients: A review Differential parental transmission of markers in BCL3 among Korean cleft case-parent trios Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms.Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs.Detection of parent-of-origin specific expression quantitative trait loci by cis-association analysis of gene expression in trios Maternal transmission effect of a PDGF-C SNP on nonsyndromic cleft lip with or without palate from a Chinese population Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1 Candidate pathway based analysis for cleft lip with or without cleft palate.Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease.Genome-wide approaches (GWA) in oral and craniofacial diseases research Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations.Hypothesis-driven candidate gene association studies: practical design and analytical considerations.Specificity protein 7 is required for proliferation and differentiation of ameloblasts and odontoblasts.Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians.

P2860

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P2860

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

http://www.wikidata.org/entity/Q33740394

description

2008 nî lūn-bûn

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2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Differential parental transmis ...... t trios from four populations.

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Differential parental transmis ...... t trios from four populations.

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Genetic Epidemiology

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Differential parental transmis ...... t trios from four populations.

@en

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Alan F Scott

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Beyoung Yun Park

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Euiju Jung

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Felicia Cheah

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Ingo Ruczinski

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Jacqueline B Hetmanski

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Jae Woong Sull

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Jiwan Park

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Kung-Yee Liang

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Margaret Daniele Fallin

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P2860

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

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

Haploview: analysis and visualization of LD and haplotype maps

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

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

Phenotypic changes in dentition of Runx2 homozygote-null mutant mice

Conservation and expression of an alternative 3' exon of Runx2 encoding a novel proline-rich C-terminal domain

Assessing maternal genetic associations: a comparison of the log-linear approach to case-parent triad data and a case-control approach.

C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers?

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505-512

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scholarly article

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10.1002/GEPI.20323

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6

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32

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Ethylin Wang Jabs

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2008-09-01T00:00:00Z

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5494040

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