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The Role of MSX1 in Human Tooth Agenesis

Journal of dental research, 2002-04, Vol.81 (4), p.274-278

2002

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TBX22 mutations are a frequent cause of cleft palate

Journal of medical genetics, 2004-01, Vol.41 (1), p.68-74

2004

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MSX1 and Orofacial Clefting with and without Tooth Agenesis

Journal of dental research, 2006-06, Vol.85 (6), p.542-546

2006

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Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Journal of medical genetics, 2008-02, Vol.45 (2), p.81-86

2008

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Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans

American journal of human genetics, 1998-08, Vol.63 (2), p.557-568

1998

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Genetic and Environmental Factors Associated with Dental Caries in Children: The Iowa Fluoride Study

Caries research, 2012-01, Vol.46 (3), p.177-184

2012

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A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

American journal of medical genetics. Part A, 2007-04, Vol.143A (8), p.846-852

2007

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Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

Journal of medical genetics, 2001-11, Vol.38 (11), p.761-766

2001

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

Birth defects research. A Clinical and molecular teratology, 2004-12, Vol.70 (12), p.893-901

2004

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Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35

American journal of human genetics, 2004-08, Vol.75 (2), p.161-173

2004

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Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines

The Cleft palate-craniofacial journal, 1997-01, Vol.34 (1), p.1-6

1997

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Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

American journal of human genetics, 2001-06, Vol.68 (6), p.1321-1326

2001

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A comparison of cranial base growth in Class I and Class II skeletal patterns

American journal of orthodontics and dentofacial orthopedics, 2001-04, Vol.119 (4), p.401-405

2001

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Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

American journal of medical genetics, 2004-03, Vol.125A (2), p.135-144

2004

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Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: Summary report from a workshop of the International Consortium for Oral Clefts genetics

The Cleft palate-craniofacial journal, 2002, Vol.39 (1), p.93-100

2002

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Homozygosity Mapping Identifies an Additional Locus for Wolfram Syndrome on Chromosome 4q

American journal of human genetics, 2000-04, Vol.66 (4), p.1229-1236

2000

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Interferon Regulatory Factor 6 (IRF6) Gene Variants and the Risk of Isolated Cleft Lip or Palate

The New England journal of medicine, 2004-08, Vol.351 (8), p.769-780

2004

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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

Teratology (Philadelphia), 1999-01, Vol.59 (1), p.39-50

1999

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Progress toward discerning the genetics of cleft lip

Current opinion in pediatrics, 2005-12, Vol.17 (6), p.731-739

2005

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Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO)

American journal of human genetics, 1993-10, Vol.53 (4), p.836-843

1993

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CRISPLD2: a novel NSCLP candidate gene

Human molecular genetics, 2008-04, Vol.17 (7), p.1061-1061

2008

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Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis

American journal of human genetics, 1992-03, Vol.50 (3), p.567-575

1992

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Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

The Cleft palate-craniofacial journal, 2003-05, Vol.40 (3), p.274-279

2003

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Detection of multiallele polymorphism within gene sequences by GC-clamped denaturing gradient gel electrophoresis

American journal of human genetics, 1992, Vol.50 (3), p.567-575

1992

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The Role of MSX1 in Human Tooth Agenesis

TBX22 mutations are a frequent cause of cleft palate

MSX1 and Orofacial Clefting with and without Tooth Agenesis

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans

Genetic and Environmental Factors Associated with Dental Caries in Children: The Iowa Fluoride Study

A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations

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

Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35

Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines

Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

A comparison of cranial base growth in Class I and Class II skeletal patterns

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: Summary report from a workshop of the International Consortium for Oral Clefts genetics

Homozygosity Mapping Identifies an Additional Locus for Wolfram Syndrome on Chromosome 4q

Interferon Regulatory Factor 6 (IRF6) Gene Variants and the Risk of Isolated Cleft Lip or Palate

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

Progress toward discerning the genetics of cleft lip

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO)

CRISPLD2: a novel NSCLP candidate gene

Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis

Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

Detection of multiallele polymorphism within gene sequences by GC-clamped denaturing gradient gel electrophoresis

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