(Q53652140)

16 May 2018

title

Family-based analysis of MSX1 haplotypes for association with oral clefts. (English)

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16 May 2018

author

Ji Wan Park

3

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16 May 2018

Roxann Ingersoll

5

object named as

Roxann Ingersoll

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16 May 2018

author name string

M Daniele Fallin

1

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16 May 2018

Jacqueline B Hetmanski

2

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16 May 2018

Alan F Scott

4

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16 May 2018

Hans A Fuernkranz

6

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16 May 2018

Iain McIntosh

7

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16 May 2018

Terri H Beaty

8

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16 May 2018

publication date

1 September 2003

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16 May 2018

published in

Genetic Epidemiology

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16 May 2018

volume

25

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16 May 2018

issue

2

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16 May 2018

page(s)

168-175

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16 May 2018

Limitations of the case-only design for identifying gene-environment interactions

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

A case-control study of nonsyndromic oral clefts in Maryland

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Rapid and reliable fluorescent cycle sequencing of double-stranded templates

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Evaluation of two putative susceptibility loci for oral clefts in the Danish population

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Nonsyndromic cleft lip and palate: complex genetics and environmental effects

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https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Likelihoods and TDT for the case-parents design.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Fluorescence detection in automated DNA sequence analysis.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10255

7 January 2021

Identifiers

DOI

10.1002/GEPI.10255

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16 May 2018

PubMed ID

12916025

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16 May 2018