Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations (Q34563506)

3 August 2017

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations (English)

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3 August 2017

Beaty TH

1

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3 August 2017

Hetmanski JB

2

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3 August 2017

Fallin MD

3

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3 August 2017

Park JW

4

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3 August 2017

Sull JW

5

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3 August 2017

McIntosh I

6

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3 August 2017

Liang KY

7

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3 August 2017

Vanderkolk CA

8

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3 August 2017

Redett RJ

9

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3 August 2017

Boyadjiev SA

10

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3 August 2017

Jabs EW

11

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3 August 2017

Chong SS

12

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3 August 2017

Cheah FS

13

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3 August 2017

Wu-Chou YH

14

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3 August 2017

Chen PK

15

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3 August 2017

Chiu YF

16

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3 August 2017

Yeow V

17

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3 August 2017

Ng IS

18

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3 August 2017

Cheng J

19

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3 August 2017

Huang S

20

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3 August 2017

Ye X

21

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3 August 2017

Wang H

22

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3 August 2017

Ingersoll R

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3 August 2017

Scott AF

24

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3 August 2017

5 September 2006

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3 August 2017

120

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https://scigraph.springernature.com/pub.10.1007/s00439-006-0235-9

3 August 2017

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Tensin1 and a previously undocumented family member, tensin2, positively regulate cell migration

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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

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Highly parallel SNP genotyping

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Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

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Contributions of PTCH gene variants to isolated cleft lip and palate

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Maternal Cigarette Smoking and Oral Clefts: A Meta-analysis

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The family based association test method: strategies for studying general genotype--phenotype associations.

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Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

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Testing candidate genes for non-syndromic oral clefts using a case-parent trio design

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12 December 2020

Association between 10 microsatellite markers and nonsyndromic cleft lip palate in the Chilean population.

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12 December 2020

Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model

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12 December 2020

Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: a reappraisal

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12 December 2020

?Mowat-Wilson? syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

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12 December 2020

A case-control study of nonsyndromic oral clefts in Maryland

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12 December 2020

Evaluation of Nyholt's procedure for multiple testing correction

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12 December 2020

Identification of SATB2 as the cleft palate gene on 2q32-q33.

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Achondroplasia is defined by recurrent G380R mutations of FGFR3

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Association between the transforming growth factor alpha gene and nonsyndromic oral clefts: a HuGE review

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Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families

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12 December 2020

A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis

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12 December 2020

Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey

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12 December 2020

Asian oral-facial cleft birth prevalence

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Holoprosencephaly: a family showing dominant inheritance and variable expression

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12 December 2020

Application of transmission disequilibrium tests to nonsyndromic oral clefts: Including candidate genes and environmental exposures in the models

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12 December 2020

HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.

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12 December 2020

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

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12 December 2020

Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: assessing gene-environment interactions in case-parent triads

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12 December 2020

Oral clefts, maternal smoking, and TGFA: a meta-analysis of gene-environment interaction

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12 December 2020

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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12 December 2020

Tobacco smoking and oral clefts: a meta-analysis.

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12 December 2020

Basement membrane collagen in the kidney: regional localization of novel chains related to collagen IV

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A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

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

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12 December 2020

Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysis.

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12 December 2020

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

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12 December 2020

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2

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12 December 2020

"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

1 reference

12 December 2020

10.1007/S00439-006-0235-9

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

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