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Kenneth N Rosenbaum

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

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Advances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|July 31, 2015
Important Considerations in the Initial Clinical Evaluation of the Dysmorphic NeonatePatroula Smpokou, Brendan C Lanpher, Kenneth N Rosenbaum
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly due to numeric chromosome abnormalitiesBenjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, et al.
Pediatric Neurology|September 13, 2011
Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I studyMaria T Acosta, Peter G Kardel, Karin S Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2006
Quantitative dysmorphology assessment in Fabry diseaseMarkus Ries, David F Moore, Chevalia J Robinson, et al.
Paediatric Anaesthesia|January 11, 2016
Preoperative evaluation and comprehensive risk assessment for children with Down syndromeAmy Feldman Lewanda, Andrew Matisoff, Mary Revenis, et al.
JAMA Ophthalmology|January 18, 2014
Handheld optical coherence tomography during sedation in young children with optic pathway gliomasRobert A Avery, Eugene I Hwang, Hiroshi Ishikawa, et al.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
Journal of Medical Genetics|December 20, 2011
Further clinical and molecular delineation of the 15q24 microdeletion syndromeHeather C Mefford, Jill A Rosenfeld, Natasha Shur, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
Pageof 1

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

Sort By:
Pageof 1
Advances in Neonatal Care : Official Journal of the National Association of Neonatal Nurses|July 31, 2015
Important Considerations in the Initial Clinical Evaluation of the Dysmorphic NeonatePatroula Smpokou, Brendan C Lanpher, Kenneth N Rosenbaum
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly due to numeric chromosome abnormalitiesBenjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, et al.
Pediatric Neurology|September 13, 2011
Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I studyMaria T Acosta, Peter G Kardel, Karin S Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2006
Quantitative dysmorphology assessment in Fabry diseaseMarkus Ries, David F Moore, Chevalia J Robinson, et al.
Paediatric Anaesthesia|January 11, 2016
Preoperative evaluation and comprehensive risk assessment for children with Down syndromeAmy Feldman Lewanda, Andrew Matisoff, Mary Revenis, et al.
JAMA Ophthalmology|January 18, 2014
Handheld optical coherence tomography during sedation in young children with optic pathway gliomasRobert A Avery, Eugene I Hwang, Hiroshi Ishikawa, et al.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
Journal of Medical Genetics|December 20, 2011
Further clinical and molecular delineation of the 15q24 microdeletion syndromeHeather C Mefford, Jill A Rosenfeld, Natasha Shur, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
Pageof 1