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David A Stevenson

Showing results (41-50 of 166) with videos related to

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American Journal of Medical Genetics. Part A|March 27, 2014
L1CAM whole gene deletion in a child with L1 syndromeBrandalyn A Chidsey, Erin E Baldwin, Reha Toydemir, et al.
Journal of Pediatric Orthopedics|September 25, 2008
Bone mineral density in children with neurofibromatosis type 1David A Stevenson, Mary Murray, David H Viskochil, et al.
Journal of Pediatric Orthopedics|July 2, 2009
Familial predisposition to developmental dysplasia of the hipDavid A Stevenson, Geraldine Mineau, Richard A Kerber, et al.
European Journal of Medical Genetics|December 28, 2011
RASA1 analysis: clinical and molecular findings in a series of consecutive casesWhitney Wooderchak-Donahue, David A Stevenson, Jamie McDonald, et al.
Frontiers in Genetics|February 13, 2015
Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new eraJamie McDonald, Whitney Wooderchak-Donahue, Chad VanSant Webb, et al.
The Journal of Pediatrics|December 8, 2004
4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotypeDavid A Stevenson, John C Carey, Brett C Cowley, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 26, 2017
Quantitative Ultrasound and Tibial Dysplasia in Neurofibromatosis Type 1David A Stevenson, Heather Hanson, Austin Stevens, et al.
American Journal of Medical Genetics. Part A|April 14, 2017
Variable clinical course of identical twin neonates with Alström syndrome presenting coincidentally with dilated cardiomyopathySeth A Hollander, Norah Alsaleh, Maura Ruzhnikov, et al.
Human Movement Science|September 13, 2011
Lower extremity strength and hopping and jumping ground reaction forces in children with neurofibromatosis type 1Barbara A Johnson, Bruce Macwilliams, John C Carey, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 31, 2018
PTPN11 Gain-of-Function Mutations Affect the Developing Human Brain, Memory, and AttentionEmily M Johnson, Alexandra D Ishak, Paige E Naylor, et al.
Pageof 17

Showing results (41-50 of 166) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics. Part A|March 27, 2014
L1CAM whole gene deletion in a child with L1 syndromeBrandalyn A Chidsey, Erin E Baldwin, Reha Toydemir, et al.
Journal of Pediatric Orthopedics|September 25, 2008
Bone mineral density in children with neurofibromatosis type 1David A Stevenson, Mary Murray, David H Viskochil, et al.
Journal of Pediatric Orthopedics|July 2, 2009
Familial predisposition to developmental dysplasia of the hipDavid A Stevenson, Geraldine Mineau, Richard A Kerber, et al.
European Journal of Medical Genetics|December 28, 2011
RASA1 analysis: clinical and molecular findings in a series of consecutive casesWhitney Wooderchak-Donahue, David A Stevenson, Jamie McDonald, et al.
Frontiers in Genetics|February 13, 2015
Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new eraJamie McDonald, Whitney Wooderchak-Donahue, Chad VanSant Webb, et al.
The Journal of Pediatrics|December 8, 2004
4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotypeDavid A Stevenson, John C Carey, Brett C Cowley, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 26, 2017
Quantitative Ultrasound and Tibial Dysplasia in Neurofibromatosis Type 1David A Stevenson, Heather Hanson, Austin Stevens, et al.
American Journal of Medical Genetics. Part A|April 14, 2017
Variable clinical course of identical twin neonates with Alström syndrome presenting coincidentally with dilated cardiomyopathySeth A Hollander, Norah Alsaleh, Maura Ruzhnikov, et al.
Human Movement Science|September 13, 2011
Lower extremity strength and hopping and jumping ground reaction forces in children with neurofibromatosis type 1Barbara A Johnson, Bruce Macwilliams, John C Carey, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 31, 2018
PTPN11 Gain-of-Function Mutations Affect the Developing Human Brain, Memory, and AttentionEmily M Johnson, Alexandra D Ishak, Paige E Naylor, et al.
Pageof 17