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Andrew C Lidral

Showing results (1-10 of 34) with videos related to

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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 modelAndrew C Lidral, Jeffrey C Murray
Current Opinion in Pediatrics|November 12, 2005
Progress toward discerning the genetics of cleft lipAndrew 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 programsHiroyuki 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 mechanismsRulang Jiang, Jeffrey O Bush, Andrew C Lidral
Seminars in Orthodontics|June 4, 2009
Genetic Factors and Orofacial CleftingAndrew 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 testDiana 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 populationEdward 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 regionRebecca 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 agenesisAlexandre 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 cleftingHuan Liu, Elizabeth J Leslie, Jenna C Carlson, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 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 modelAndrew C Lidral, Jeffrey C Murray
Current Opinion in Pediatrics|November 12, 2005
Progress toward discerning the genetics of cleft lipAndrew 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 programsHiroyuki 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 mechanismsRulang Jiang, Jeffrey O Bush, Andrew C Lidral
Seminars in Orthodontics|June 4, 2009
Genetic Factors and Orofacial CleftingAndrew 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 testDiana 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 populationEdward 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 regionRebecca 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 agenesisAlexandre 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 cleftingHuan Liu, Elizabeth J Leslie, Jenna C Carlson, et al.
Pageof 4