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Nathaniel H Robin

Showing results (81-90 of 118) with videos related to

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American Journal of Medical Genetics. Part A|September 15, 2018
A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13CJariya Upadia, Patrick R Gonzales, T Prescott Atkinson, et al.
Southern Medical Journal|November 15, 2006
The multidisciplinary evaluation and management of cleft lip and palateNathaniel H Robin, Heather Baty, Judith Franklin, et al.
Annals of Plastic Surgery|April 9, 2021
Mandibular Distraction Osteogenesis as a Primary Intervention in Infants With Pierre Robin SequenceEdgar Soto, Shivani Ananthasekar, Srikanth Kurapati, et al.
Neurotoxicology and Teratology|November 22, 2005
Dysmorphic and anthropometric outcomes in 6-year-old prenatally cocaine-exposed childrenSonia Minnes, Nathaniel H Robin, April A Alt, et al.
American Journal of Medical Genetics. Part A|January 6, 2016
Trisomy 18: A single-center evaluation of management trends and experience with aggressive obstetric or neonatal interventionAkila Subramaniam, Adam P Jacobs, Ying Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2022
Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Marilyn M Li, Ahmad Abou Tayoun, Marina DiStefano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
AsktheGeneticist: five years of online experienceCatherine Tesla, Bruce R Korf, Lynn Holt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 15, 2013
The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization systemFady M Mikhail, Rachel D Burnside, Brooke Rush, et al.
American Journal of Medical Genetics. Part A|January 18, 2022
Near complete deletion of KMT2D in a college studentCatherine Gooch, Jaclyn Paige Souder, Matthew L Tedder, et al.
American Journal of Medical Genetics. Part A|October 28, 2011
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disordersFady M Mikhail, Edward J Lose, Nathaniel H Robin, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics. Part A|September 15, 2018
A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13CJariya Upadia, Patrick R Gonzales, T Prescott Atkinson, et al.
Southern Medical Journal|November 15, 2006
The multidisciplinary evaluation and management of cleft lip and palateNathaniel H Robin, Heather Baty, Judith Franklin, et al.
Annals of Plastic Surgery|April 9, 2021
Mandibular Distraction Osteogenesis as a Primary Intervention in Infants With Pierre Robin SequenceEdgar Soto, Shivani Ananthasekar, Srikanth Kurapati, et al.
Neurotoxicology and Teratology|November 22, 2005
Dysmorphic and anthropometric outcomes in 6-year-old prenatally cocaine-exposed childrenSonia Minnes, Nathaniel H Robin, April A Alt, et al.
American Journal of Medical Genetics. Part A|January 6, 2016
Trisomy 18: A single-center evaluation of management trends and experience with aggressive obstetric or neonatal interventionAkila Subramaniam, Adam P Jacobs, Ying Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2022
Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Marilyn M Li, Ahmad Abou Tayoun, Marina DiStefano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
AsktheGeneticist: five years of online experienceCatherine Tesla, Bruce R Korf, Lynn Holt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 15, 2013
The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization systemFady M Mikhail, Rachel D Burnside, Brooke Rush, et al.
American Journal of Medical Genetics. Part A|January 18, 2022
Near complete deletion of KMT2D in a college studentCatherine Gooch, Jaclyn Paige Souder, Matthew L Tedder, et al.
American Journal of Medical Genetics. Part A|October 28, 2011
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disordersFady M Mikhail, Edward J Lose, Nathaniel H Robin, et al.
Pageof 12