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Steven B Bleyl

Showing results (1-10 of 44) with videos related to

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Pediatric Neurology|April 19, 2014
Clinical exome sequencing identifies a novel TUBB4A mutation in a child with static hypomyelinating leukodystrophyShawn M Purnell, Steven B Bleyl, Joshua L Bonkowsky
American Journal of Medical Genetics. Part A|August 21, 2007
Two unique patients with novel microdeletions in 4p16.3 that exclude the WHS critical regions: implications for critical region designationSarah T South, Steven B Bleyl, John C Carey
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 6, 2011
Detection of isoform-specific fibroblast growth factor receptors by whole-mount in situ hybridization in early chick embryosJunko Nishita, Sho Ohta, Steven B Bleyl, et al.
Future Cardiology|July 10, 2013
Family-based studies to identify genetic variants that cause congenital heart defectsCammon B Arrington, Steven B Bleyl, Luca Brunelli, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|June 21, 2006
Restricted expression of Fgf16 within the developing chick inner earSusan C Chapman, Qin Cai, Steven B Bleyl, et al.
Gene Expression Patterns : GEP|November 17, 2009
Identification of differentially expressed genes in early inner ear developmentChristian N Paxton, Steven B Bleyl, Susan C Chapman, et al.
European Journal of Medical Genetics|March 20, 2012
Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defectsCammon B Arrington, Benjamin R Dowse, Steven B Bleyl, et al.
The Journal of Pediatrics|September 2, 2015
Turner Syndrome in Girls Presenting with Coarctation of the AortaAaron Eckhauser, Sarah T South, Lindsay Meyers, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene clusterDavid A Stevenson, Steven B Bleyl, Teresa Maxwell, et al.
Pediatrics|June 3, 2015
Progressive Aortic Dilation Associated With ACTA2 Mutations Presenting in InfancyAnji T Yetman, Lois J Starr, Steven B Bleyl, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Pediatric Neurology|April 19, 2014
Clinical exome sequencing identifies a novel TUBB4A mutation in a child with static hypomyelinating leukodystrophyShawn M Purnell, Steven B Bleyl, Joshua L Bonkowsky
American Journal of Medical Genetics. Part A|August 21, 2007
Two unique patients with novel microdeletions in 4p16.3 that exclude the WHS critical regions: implications for critical region designationSarah T South, Steven B Bleyl, John C Carey
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 6, 2011
Detection of isoform-specific fibroblast growth factor receptors by whole-mount in situ hybridization in early chick embryosJunko Nishita, Sho Ohta, Steven B Bleyl, et al.
Future Cardiology|July 10, 2013
Family-based studies to identify genetic variants that cause congenital heart defectsCammon B Arrington, Steven B Bleyl, Luca Brunelli, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|June 21, 2006
Restricted expression of Fgf16 within the developing chick inner earSusan C Chapman, Qin Cai, Steven B Bleyl, et al.
Gene Expression Patterns : GEP|November 17, 2009
Identification of differentially expressed genes in early inner ear developmentChristian N Paxton, Steven B Bleyl, Susan C Chapman, et al.
European Journal of Medical Genetics|March 20, 2012
Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defectsCammon B Arrington, Benjamin R Dowse, Steven B Bleyl, et al.
The Journal of Pediatrics|September 2, 2015
Turner Syndrome in Girls Presenting with Coarctation of the AortaAaron Eckhauser, Sarah T South, Lindsay Meyers, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene clusterDavid A Stevenson, Steven B Bleyl, Teresa Maxwell, et al.
Pediatrics|June 3, 2015
Progressive Aortic Dilation Associated With ACTA2 Mutations Presenting in InfancyAnji T Yetman, Lois J Starr, Steven B Bleyl, et al.
Pageof 5