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Kelly A Bear

Showing results (1-10 of 9) with videos related to

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American Journal of Medical Genetics. Part A|May 15, 2015
GLI2 mutations typically result in pituitary anomalies with or without postaxial polydactylyKelly A Bear, Benjamin D Solomon
Journal of Travel Medicine|July 20, 2010
Disparities exist in the availability of outpatient malaria treatment in Maryland, USAKelly A Bear, Amanda I Higginson, Patrick W Hickey
Proceedings of the National Academy of Sciences of the United States of America|May 23, 2013
Clinical genomic databaseBenjamin D Solomon, Anh-Dao Nguyen, Kelly A Bear, et al.
Clinical Dysmorphology|February 23, 2012
Evidence for SHH as a candidate gene for encephaloceleKelly A Bear, Benjamin D Solomon, Erich Roessler, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|October 3, 2020
Fingertip ultrasound evaluation of umbilical catheter position in the neonatal intensive care unit compared to conventional ultrasound radiography: a preliminary investigationJonathan R Wood, Neil R Halonen, Kelly A Bear, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, 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.
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.
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 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|May 15, 2015
GLI2 mutations typically result in pituitary anomalies with or without postaxial polydactylyKelly A Bear, Benjamin D Solomon
Journal of Travel Medicine|July 20, 2010
Disparities exist in the availability of outpatient malaria treatment in Maryland, USAKelly A Bear, Amanda I Higginson, Patrick W Hickey
Proceedings of the National Academy of Sciences of the United States of America|May 23, 2013
Clinical genomic databaseBenjamin D Solomon, Anh-Dao Nguyen, Kelly A Bear, et al.
Clinical Dysmorphology|February 23, 2012
Evidence for SHH as a candidate gene for encephaloceleKelly A Bear, Benjamin D Solomon, Erich Roessler, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|October 3, 2020
Fingertip ultrasound evaluation of umbilical catheter position in the neonatal intensive care unit compared to conventional ultrasound radiography: a preliminary investigationJonathan R Wood, Neil R Halonen, Kelly A Bear, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, 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.
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.
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 1