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Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 4, 2004
Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model
Andrew C Lidral, Jeffrey C Murray
Current Opinion in Pediatrics
|
November 12, 2005
Progress toward discerning the genetics of cleft lip
Andrew C Lidral, Lina M Moreno
BMC Bioinformatics
|
June 27, 2008
Application of the Linux cluster for exhaustive window haplotype analysis using the FBAT and Unphased programs
Hiroyuki Mishima, Andrew C Lidral, Jun Ni
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 18, 2005
Development of the upper lip: morphogenetic and molecular mechanisms
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral
Seminars in Orthodontics
|
June 4, 2009
Genetic Factors and Orofacial Clefting
Andrew C Lidral, Lina M Moreno, Steven A Bullard
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 26, 2006
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
Diana M Juriloff, Muriel J Harris, Andrew P McMahon, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Genetic variation of FOXE1 and risk for orofacial clefts in a California population
Edward J Lammer, Nebil Mohammed, David M Iovannisci, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
May 8, 2003
Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region
Rebecca L Slayton, Laura Williams, Jeffrey C Murray, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis
Alexandre R Vieira, Adriana Modesto, Raquel Meira, et al.
Nature Communications
|
March 14, 2017
Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting
Huan Liu, Elizabeth J Leslie, Jenna C Carlson, et al.
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of 4
Search research articles
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Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 4, 2004
Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model
Andrew C Lidral, Jeffrey C Murray
Current Opinion in Pediatrics
|
November 12, 2005
Progress toward discerning the genetics of cleft lip
Andrew C Lidral, Lina M Moreno
BMC Bioinformatics
|
June 27, 2008
Application of the Linux cluster for exhaustive window haplotype analysis using the FBAT and Unphased programs
Hiroyuki Mishima, Andrew C Lidral, Jun Ni
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 18, 2005
Development of the upper lip: morphogenetic and molecular mechanisms
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral
Seminars in Orthodontics
|
June 4, 2009
Genetic Factors and Orofacial Clefting
Andrew C Lidral, Lina M Moreno, Steven A Bullard
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 26, 2006
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
Diana M Juriloff, Muriel J Harris, Andrew P McMahon, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Genetic variation of FOXE1 and risk for orofacial clefts in a California population
Edward J Lammer, Nebil Mohammed, David M Iovannisci, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
May 8, 2003
Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region
Rebecca L Slayton, Laura Williams, Jeffrey C Murray, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis
Alexandre R Vieira, Adriana Modesto, Raquel Meira, et al.
Nature Communications
|
March 14, 2017
Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting
Huan Liu, Elizabeth J Leslie, Jenna C Carlson, et al.
Page
of 4