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Omar A Abdul-Rahman

Showing results (1-10 of 43) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2006
The diagnostic utility of a genetics evaluation in children with pervasive developmental disordersOmar A Abdul-Rahman, Louanne Hudgins
Current Opinion in Pediatrics|October 12, 2021
Fetal alcohol spectrum disorders: current state of diagnosis and treatmentDiego A Gomez, Omar A Abdul-Rahman
Medical Hypotheses|February 1, 2012
An immunological basis of hyperphagia driven by GABAergic dysfunction in Prader-Willi SyndromeUjjwal Rout, Omar A Abdul-Rahman, Dirk Marcel Dhossche
Journal of Pediatric Hematology/Oncology|July 31, 2004
Cryptococcal sepsis diagnosed by bone marrow examinationOmar A Abdul-Rahman, Hannah Gay, Elizabeth Caldwell, et al.
American Journal of Medical Genetics. Part A|June 12, 2020
Differentiating molecular etiologies of Angelman syndrome through facial phenotyping using deep learningDiego A Gomez, Lynne M Bird, Nicole Fleischer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 29, 2008
Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblingsMatthew Vanlandingham, Tuan V Nguyen, Omar A Abdul-Rahman, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Van den Ende-Gupta syndrome: laryngeal abnormalities in two siblingsChristopher W Carr, Jeffrey D Carron, Ralph S Lachman, et al.
Journal of Pediatric Hematology/Oncology|July 1, 2009
Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1betaOmar A Abdul-Rahman, Emma L Edghill, Andrea Kwan, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2CChristopher W Carr, Holly H Zimmerman, Christa Lese Martin, et al.
Pediatrics|December 18, 2013
A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosisBrittany N Simpson, Nancy Hogg, Lena M Svensson, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2006
The diagnostic utility of a genetics evaluation in children with pervasive developmental disordersOmar A Abdul-Rahman, Louanne Hudgins
Current Opinion in Pediatrics|October 12, 2021
Fetal alcohol spectrum disorders: current state of diagnosis and treatmentDiego A Gomez, Omar A Abdul-Rahman
Medical Hypotheses|February 1, 2012
An immunological basis of hyperphagia driven by GABAergic dysfunction in Prader-Willi SyndromeUjjwal Rout, Omar A Abdul-Rahman, Dirk Marcel Dhossche
Journal of Pediatric Hematology/Oncology|July 31, 2004
Cryptococcal sepsis diagnosed by bone marrow examinationOmar A Abdul-Rahman, Hannah Gay, Elizabeth Caldwell, et al.
American Journal of Medical Genetics. Part A|June 12, 2020
Differentiating molecular etiologies of Angelman syndrome through facial phenotyping using deep learningDiego A Gomez, Lynne M Bird, Nicole Fleischer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 29, 2008
Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblingsMatthew Vanlandingham, Tuan V Nguyen, Omar A Abdul-Rahman, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Van den Ende-Gupta syndrome: laryngeal abnormalities in two siblingsChristopher W Carr, Jeffrey D Carron, Ralph S Lachman, et al.
Journal of Pediatric Hematology/Oncology|July 1, 2009
Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1betaOmar A Abdul-Rahman, Emma L Edghill, Andrea Kwan, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2CChristopher W Carr, Holly H Zimmerman, Christa Lese Martin, et al.
Pediatrics|December 18, 2013
A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosisBrittany N Simpson, Nancy Hogg, Lena M Svensson, et al.
Pageof 5