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Nancy B Spinner

Showing results (21-30 of 140) with videos related to

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Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|July 28, 2006
Familial stenosis of the pulmonary artery branches with a JAG1 mutationAna Berta Sousa, Ana Medeira, Binita M Kamath, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 13, 2007
Interlobular bile duct loss in pediatric cholestatic disease is associated with aberrant cytokeratin 7 expression by hepatocytesLinda M Ernst, Nancy B Spinner, David A Piccoli, et al.
Case Reports in Genetics|October 24, 2013
Persistent mosaicism for 12p duplication/triplication chromosome structural abnormality in peripheral bloodAmy L Shackelford, Laura K Conlin, Marybeth Hummel, et al.
Frontiers in Pediatrics|August 1, 2020
Genomic Diagnosis for Pediatric Disorders: Revolution and EvolutionEmilie Lalonde, Stefan Rentas, Fumin Lin, et al.
American Journal of Medical Genetics|September 24, 2002
Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordanceBinita M Kamath, Ian D Krantz, Nancy B Spinner, et al.
Journal of Genetic Counseling|September 17, 2013
A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practiceMarian Reiff, Rebecca Mueller, Surabhi Mulchandani, et al.
Prenatal Diagnosis|March 28, 2017
Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory ConsiderationsAhmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Significant liver disease in a patient with Y116H mutation in the MVK geneMelissa Leyva-Vega, Pamela F Weiss, Jaya Ganesh, et al.
The American Journal of Surgical Pathology|May 18, 2005
Peripheral bile duct paucity and cholestasis in the liver of a patient with Alagille syndrome: further evidence supporting a lack of postnatal bile duct branching and elongationLouis Libbrecht, Nancy B Spinner, Elizabeth C Moore, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
An 18-year follow-up report on an infant with a duplication of 9q34Erin L Youngs, Timothy McCord, Jessica A Hellings, et al.
Pageof 14

Showing results (21-30 of 140) with videos related to

Sort By:
Pageof 14
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|July 28, 2006
Familial stenosis of the pulmonary artery branches with a JAG1 mutationAna Berta Sousa, Ana Medeira, Binita M Kamath, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 13, 2007
Interlobular bile duct loss in pediatric cholestatic disease is associated with aberrant cytokeratin 7 expression by hepatocytesLinda M Ernst, Nancy B Spinner, David A Piccoli, et al.
Case Reports in Genetics|October 24, 2013
Persistent mosaicism for 12p duplication/triplication chromosome structural abnormality in peripheral bloodAmy L Shackelford, Laura K Conlin, Marybeth Hummel, et al.
Frontiers in Pediatrics|August 1, 2020
Genomic Diagnosis for Pediatric Disorders: Revolution and EvolutionEmilie Lalonde, Stefan Rentas, Fumin Lin, et al.
American Journal of Medical Genetics|September 24, 2002
Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordanceBinita M Kamath, Ian D Krantz, Nancy B Spinner, et al.
Journal of Genetic Counseling|September 17, 2013
A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practiceMarian Reiff, Rebecca Mueller, Surabhi Mulchandani, et al.
Prenatal Diagnosis|March 28, 2017
Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory ConsiderationsAhmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Significant liver disease in a patient with Y116H mutation in the MVK geneMelissa Leyva-Vega, Pamela F Weiss, Jaya Ganesh, et al.
The American Journal of Surgical Pathology|May 18, 2005
Peripheral bile duct paucity and cholestasis in the liver of a patient with Alagille syndrome: further evidence supporting a lack of postnatal bile duct branching and elongationLouis Libbrecht, Nancy B Spinner, Elizabeth C Moore, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
An 18-year follow-up report on an infant with a duplication of 9q34Erin L Youngs, Timothy McCord, Jessica A Hellings, et al.
Pageof 14