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Virginia P Sybert

Showing results (11-20 of 30) with videos related to

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The Journal of Investigative Dermatology|May 14, 2004
Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichiaAmy Y Jan, Shivan Amin, Paulina Ratajczak, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndromeMeena R Julapalli, Richard K Scher, Virginia P Sybert, et al.
Hormone Research|June 8, 2002
Growth failure in early life: an important manifestation of Turner syndromeMichael L Davenport, Natavut Punyasavatsut, Paul W Stewart, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
Phenotype and X inactivation in 45,X/46,X,r(X) casesKathleen A Leppig, Virginia P Sybert, Judith L Ross, et al.
Pediatrics|August 3, 2005
Growth characteristics of children with ectodermal dysplasia syndromesKathleen J Motil, Timothy J Fete, J Kennard Fraley, et al.
Pediatric Dermatology|December 23, 2014
Ventral midline blanching in the setting of segmental infantile hemangiomas: clinical observations and pathogenetic implicationsDana F Feigenbaum, Virginia P Sybert, Sheryll L Vanderhooft, et al.
American Journal of Human Genetics|August 18, 2015
A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen SyndromeJennifer J Johnston, Monica Y Sanchez-Contreras, Kim M Keppler-Noreuil, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
The Journal of Investigative Dermatology|March 22, 2003
Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlationsGabriele Richard, Nkecha Brown, Fatima Rouan, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndromeMary Fete, Hans vanBokhoven, Suzanne E Clements, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
The Journal of Investigative Dermatology|May 14, 2004
Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichiaAmy Y Jan, Shivan Amin, Paulina Ratajczak, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndromeMeena R Julapalli, Richard K Scher, Virginia P Sybert, et al.
Hormone Research|June 8, 2002
Growth failure in early life: an important manifestation of Turner syndromeMichael L Davenport, Natavut Punyasavatsut, Paul W Stewart, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
Phenotype and X inactivation in 45,X/46,X,r(X) casesKathleen A Leppig, Virginia P Sybert, Judith L Ross, et al.
Pediatrics|August 3, 2005
Growth characteristics of children with ectodermal dysplasia syndromesKathleen J Motil, Timothy J Fete, J Kennard Fraley, et al.
Pediatric Dermatology|December 23, 2014
Ventral midline blanching in the setting of segmental infantile hemangiomas: clinical observations and pathogenetic implicationsDana F Feigenbaum, Virginia P Sybert, Sheryll L Vanderhooft, et al.
American Journal of Human Genetics|August 18, 2015
A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen SyndromeJennifer J Johnston, Monica Y Sanchez-Contreras, Kim M Keppler-Noreuil, et al.
Genes|December 23, 2022
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly UpdateNicolai Peschel, John T Wright, Maranke I Koster, et al.
The Journal of Investigative Dermatology|March 22, 2003
Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlationsGabriele Richard, Nkecha Brown, Fatima Rouan, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndromeMary Fete, Hans vanBokhoven, Suzanne E Clements, et al.
Pageof 3