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Andrew C Lidral

Showing results (21-30 of 34) with videos related to

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European Journal of Human Genetics : EJHG|December 19, 2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/PSun J Choi, Mary L Marazita, P Suzanne Hart, et al.
Human Heredity|June 13, 2009
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsMary L Marazita, Andrew C Lidral, Jeffrey C Murray, et al.
American Journal of Human Genetics|March 3, 2009
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lipSatoshi Suzuki, Mary L Marazita, Margaret E Cooper, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Nature Genetics|September 10, 2002
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromesShinji Kondo, Brian C Schutte, Rebecca J Richardson, et al.
The New England Journal of Medicine|August 20, 2004
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palateTheresa M Zucchero, Margaret E Cooper, Brion S Maher, et al.
American Journal of Human Genetics|June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.
American Journal of Medical Genetics. Part A|February 8, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Soumya Rao, Sandra von Hardenberg, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
American Journal of Human Genetics|February 24, 2015
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS lociElizabeth J Leslie, Margaret A Taub, Huan Liu, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|December 19, 2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/PSun J Choi, Mary L Marazita, P Suzanne Hart, et al.
Human Heredity|June 13, 2009
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsMary L Marazita, Andrew C Lidral, Jeffrey C Murray, et al.
American Journal of Human Genetics|March 3, 2009
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lipSatoshi Suzuki, Mary L Marazita, Margaret E Cooper, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Nature Genetics|September 10, 2002
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromesShinji Kondo, Brian C Schutte, Rebecca J Richardson, et al.
The New England Journal of Medicine|August 20, 2004
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palateTheresa M Zucchero, Margaret E Cooper, Brion S Maher, et al.
American Journal of Human Genetics|June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.
American Journal of Medical Genetics. Part A|February 8, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Soumya Rao, Sandra von Hardenberg, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
American Journal of Human Genetics|February 24, 2015
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS lociElizabeth J Leslie, Margaret A Taub, Huan Liu, et al.
Pageof 4