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Pedro A Sanchez

Showing results (41-50 of 100) with videos related to

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American Journal of Human Genetics|June 15, 2006
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathwayRyan McDaniell, Daniel M Warthen, Pedro A Sanchez-Lara, et al.
Development (Cambridge, England)|February 6, 2014
TGFβ regulates epithelial-mesenchymal interactions through WNT signaling activity to control muscle development in the soft palateJun-ichi Iwata, Akiko Suzuki, Toshiaki Yokota, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Fetal constraint as a potential risk factor for craniosynostosisPedro A Sanchez-Lara, Suzan L Carmichael, John M Graham, et al.
Plastic and Reconstructive Surgery|December 28, 2018
Risk Factors for Preoperative Developmental Delay in Patients with Nonsyndromic Sagittal CraniosynostosisThomas A Imahiyerobo, Alexis L Johns, Eisha A Christian, et al.
Development (Cambridge, England)|February 15, 2013
Smad4-Irf6 genetic interaction and TGFβ-mediated IRF6 signaling cascade are crucial for palatal fusion in miceJun-ichi Iwata, Akiko Suzuki, Richard C Pelikan, et al.
Molecular Genetics and Metabolism|November 25, 2010
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorderLinda M Randolph, Hollie A Jackson, Jing Wang, et al.
BMC Medical Genetics|March 23, 2012
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literatureTom B Davidson, Pedro A Sanchez-Lara, Linda M Randolph, et al.
Clinical Epidemiology|August 11, 2012
Hypertrophic scarring in cleft lip repair: a comparison of incidence among ethnic groupsAli M Soltani, Cameron S Francis, Arash Motamed, et al.
Genes|August 14, 2020
A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and PalateBeau Sylvester, Frederick Brindopke, Akiko Suzuki, et al.
Human Molecular Genetics|January 11, 2017
Intraflagellar transport 88 (IFT88) is crucial for craniofacial development in mice and is a candidate gene for human cleft lip and palateHua Tian, Jifan Feng, Jingyuan Li, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|June 15, 2006
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathwayRyan McDaniell, Daniel M Warthen, Pedro A Sanchez-Lara, et al.
Development (Cambridge, England)|February 6, 2014
TGFβ regulates epithelial-mesenchymal interactions through WNT signaling activity to control muscle development in the soft palateJun-ichi Iwata, Akiko Suzuki, Toshiaki Yokota, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Fetal constraint as a potential risk factor for craniosynostosisPedro A Sanchez-Lara, Suzan L Carmichael, John M Graham, et al.
Plastic and Reconstructive Surgery|December 28, 2018
Risk Factors for Preoperative Developmental Delay in Patients with Nonsyndromic Sagittal CraniosynostosisThomas A Imahiyerobo, Alexis L Johns, Eisha A Christian, et al.
Development (Cambridge, England)|February 15, 2013
Smad4-Irf6 genetic interaction and TGFβ-mediated IRF6 signaling cascade are crucial for palatal fusion in miceJun-ichi Iwata, Akiko Suzuki, Richard C Pelikan, et al.
Molecular Genetics and Metabolism|November 25, 2010
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorderLinda M Randolph, Hollie A Jackson, Jing Wang, et al.
BMC Medical Genetics|March 23, 2012
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literatureTom B Davidson, Pedro A Sanchez-Lara, Linda M Randolph, et al.
Clinical Epidemiology|August 11, 2012
Hypertrophic scarring in cleft lip repair: a comparison of incidence among ethnic groupsAli M Soltani, Cameron S Francis, Arash Motamed, et al.
Genes|August 14, 2020
A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and PalateBeau Sylvester, Frederick Brindopke, Akiko Suzuki, et al.
Human Molecular Genetics|January 11, 2017
Intraflagellar transport 88 (IFT88) is crucial for craniofacial development in mice and is a candidate gene for human cleft lip and palateHua Tian, Jifan Feng, Jingyuan Li, et al.
Pageof 10