Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations (Q33740394)

29 July 2017

title

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

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29 July 2017

Ethylin Wang Jabs

14

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Sun Ha Jee

object named as

Sun Ha Jee

13

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Philip Kuo-Ting Chen

8

object named as

Philip K Chen

1 reference

29 July 2017

12

Beyoung Yun Park

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29 July 2017

Jae Woong Sull

1

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29 July 2017

Kung-Yee Liang

2

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29 July 2017

Jacqueline B Hetmanski

3

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29 July 2017

Margaret Daniele Fallin

4

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29 July 2017

Roxann G Ingersoll

5

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29 July 2017

Jiwan Park

6

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29 July 2017

Yah-Huei Wu-Chou

7

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29 July 2017

Samuel S Chong

9

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29 July 2017

Felicia Cheah

10

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29 July 2017

Vincent Yeow

11

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29 July 2017

Richard Redett

15

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29 July 2017

Euiju Jung

16

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29 July 2017

Ingo Ruczinski

17

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29 July 2017

Alan F Scott

18

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29 July 2017

Terri H Beaty

19

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29 July 2017

publication date

1 September 2008

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29 July 2017

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29 July 2017

volume

32

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29 July 2017

issue

6

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29 July 2017

page(s)

505-512

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Human genetic factors in nonsyndromic cleft lip and palate: an update

29 July 2017

cites work

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Mitotic retention of gene expression patterns by the cell fate-determining transcription factor Runx2.

21 June 2018

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Runx2 regulates the expression of GNAS on SaOs-2 cells.

21 June 2018

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A hybrid design for studying genetic influences on risk of diseases with onset early in life

21 June 2018

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

21 June 2018

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Minireview: GNAS: normal and abnormal functions.

21 June 2018

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

21 June 2018

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21 June 2018

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

21 June 2018

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Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

21 June 2018

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The complex genetics of cleft lip and palate

21 June 2018

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Phenotypic changes in dentition of Runx2 homozygote-null mutant mice

21 June 2018

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What good is genomic imprinting: the function of parent-specific gene expression

21 June 2018

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

21 June 2018

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Implementing a unified approach to family-based tests of association.

21 June 2018

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

21 June 2018

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Testing for linkage disequilibrium, maternal effects, and imprinting with (In)complete case-parent triads, by use of the computer program LEM.

21 June 2018

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Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

21 June 2018

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A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development

21 June 2018

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Prediction of liability to orofacial clefting using genetic and craniofacial data from parents

21 June 2018

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A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

21 June 2018

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Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 June 2018

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

21 June 2018

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

21 June 2018

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Achondroplasia is defined by recurrent G380R mutations of FGFR3

21 June 2018

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Highly parallel SNP genotyping

21 June 2018

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Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements

30 October 2018

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Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

30 October 2018

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Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads

30 October 2018

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Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

30 October 2018

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Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test.

30 October 2018

1 reference

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A natural history of cleidocranial dysplasia

30 October 2018

1 reference

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Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.

30 October 2018

1 reference

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A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

30 October 2018

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Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate

30 October 2018

1 reference

12 December 2020

Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome

1 reference

12 December 2020

BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

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12 December 2020

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

12 December 2020

Maternal Cigarette Smoking and Oral Clefts: A Meta-analysis

1 reference

12 December 2020

Identifiers

DOI

10.1002/GEPI.20323

1 reference

29 July 2017

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29 July 2017

1 reference