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Nathaniel H Robin

Showing results (91-100 of 118) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphismYunjia Chen, Ender Karaca, Nathaniel H Robin, et al.
Chest|June 25, 2008
Genetic and reproductive knowledge among adolescents and adults with cystic fibrosisGrace H Houser, Cheryl L Holt, J P Clancy, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Utilizing high-fidelity crucial conversation simulation in genetic counseling trainingR Lynn Holt, Nancy M Tofil, Christina Hurst, et al.
Clinical Ophthalmology (Auckland, N.Z.)|January 15, 2021
Stickler Syndrome (SS): Laser Prophylaxis for Retinal Detachment (Modified Ora Secunda Cerclage, OSC/SS)Robert E Morris, Edward Scott Parma, Nathaniel H Robin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
Clinical relevance of small copy-number variants in chromosomal microarray clinical testingDana Hollenbeck, Crescenda L Williams, Kathryn Drazba, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing lossRaye L Alford, Kathleen S Arnos, Michelle Fox, et al.
American Journal of Medical Genetics. Part A|August 6, 2008
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?Mahim Jain, Deeann Wallis, Nathaniel H Robin, et al.
Molecular Genetics & Genomic Medicine|April 2, 2014
Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletionYu-Wei Cheng, Christopher A Tan, Agata Minor, et al.
American Heart Journal|April 29, 2006
Intrafamilial variability of noncompaction of the ventricular myocardiumMark T Johnson, Shaoxiong Zhang, Robert Gilkeson, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)Fady M Mikhail, Achara Sathienkijkanchai, Nathaniel H Robin, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphismYunjia Chen, Ender Karaca, Nathaniel H Robin, et al.
Chest|June 25, 2008
Genetic and reproductive knowledge among adolescents and adults with cystic fibrosisGrace H Houser, Cheryl L Holt, J P Clancy, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
Utilizing high-fidelity crucial conversation simulation in genetic counseling trainingR Lynn Holt, Nancy M Tofil, Christina Hurst, et al.
Clinical Ophthalmology (Auckland, N.Z.)|January 15, 2021
Stickler Syndrome (SS): Laser Prophylaxis for Retinal Detachment (Modified Ora Secunda Cerclage, OSC/SS)Robert E Morris, Edward Scott Parma, Nathaniel H Robin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
Clinical relevance of small copy-number variants in chromosomal microarray clinical testingDana Hollenbeck, Crescenda L Williams, Kathryn Drazba, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing lossRaye L Alford, Kathleen S Arnos, Michelle Fox, et al.
American Journal of Medical Genetics. Part A|August 6, 2008
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?Mahim Jain, Deeann Wallis, Nathaniel H Robin, et al.
Molecular Genetics & Genomic Medicine|April 2, 2014
Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletionYu-Wei Cheng, Christopher A Tan, Agata Minor, et al.
American Heart Journal|April 29, 2006
Intrafamilial variability of noncompaction of the ventricular myocardiumMark T Johnson, Shaoxiong Zhang, Robert Gilkeson, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)Fady M Mikhail, Achara Sathienkijkanchai, Nathaniel H Robin, et al.
Pageof 12