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Donald W Hadley

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

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The Journal of Pediatrics|June 2, 2015
Executive Function and Adaptive Behavior in Muenke SyndromeColin M P Yarnell, Yonit A Addissie, Donald W Hadley, et al.
Pediatrics|May 16, 2012
Incidental medical information in whole-exome sequencingBenjamin D Solomon, Donald W Hadley, Daniel E Pineda-Alvarez, et al.
The Journal of Pediatrics|December 17, 2013
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) associationBenjamin D Solomon, Linda A Baker, Kelly A Bear, et al.
American Journal of Medical Genetics. Part A|January 8, 2016
Muenke syndrome: An international multicenter natural history studyPaul Kruszka, Yonit A Addissie, Colin M P Yarnell, et al.
Nature Genetics|March 9, 2004
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCORDavid Ng, Nalin Thakker, Connie M Corcoran, et al.
Molecular Genetics and Metabolism|July 20, 2011
Personalized genomic medicine: lessons from the exomeBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Journal of Medical Genetics|April 19, 2014
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephalyKelly A Bear, Benjamin D Solomon, Sonir Antonini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristicsKarin Weiss, Paul Kruszka, Maria J Guillen Sacoto, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literatureEmily S Doherty, Felicitas Lacbawan, Donald W Hadley, et al.
Journal of Medical Genetics|July 14, 2012
Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic HedgehogBenjamin D Solomon, Kelly A Bear, Adrian Wyllie, et al.
Pageof 5

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

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
The Journal of Pediatrics|June 2, 2015
Executive Function and Adaptive Behavior in Muenke SyndromeColin M P Yarnell, Yonit A Addissie, Donald W Hadley, et al.
Pediatrics|May 16, 2012
Incidental medical information in whole-exome sequencingBenjamin D Solomon, Donald W Hadley, Daniel E Pineda-Alvarez, et al.
The Journal of Pediatrics|December 17, 2013
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) associationBenjamin D Solomon, Linda A Baker, Kelly A Bear, et al.
American Journal of Medical Genetics. Part A|January 8, 2016
Muenke syndrome: An international multicenter natural history studyPaul Kruszka, Yonit A Addissie, Colin M P Yarnell, et al.
Nature Genetics|March 9, 2004
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCORDavid Ng, Nalin Thakker, Connie M Corcoran, et al.
Molecular Genetics and Metabolism|July 20, 2011
Personalized genomic medicine: lessons from the exomeBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Journal of Medical Genetics|April 19, 2014
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephalyKelly A Bear, Benjamin D Solomon, Sonir Antonini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristicsKarin Weiss, Paul Kruszka, Maria J Guillen Sacoto, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literatureEmily S Doherty, Felicitas Lacbawan, Donald W Hadley, et al.
Journal of Medical Genetics|July 14, 2012
Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic HedgehogBenjamin D Solomon, Kelly A Bear, Adrian Wyllie, et al.
Pageof 5