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H Robin

Showing results (251-260 of 297) with videos related to

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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.
Human Molecular Genetics|March 1, 1995
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndromeU Schell, A Hehr, G J Feldman, et al.
American Journal of Human Genetics|April 1, 1995
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6G J Feldman, N H Robin, L A Brueton, 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.
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Succinimide hydroxamic acids as potent inhibitors of histone deacetylase (HDAC)Michael L Curtin, Robert B Garland, H Robin Heyman, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Cryobiology|November 26, 2008
Towards cryopreservation of Greenshell mussel (Perna canaliculus) oocytesSerean L Adams, H Robin Tervit, Lindsay T McGowan, et al.
Pageof 30

Showing results (251-260 of 297) with videos related to

Sort By:
Pageof 30
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.
Human Molecular Genetics|March 1, 1995
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndromeU Schell, A Hehr, G J Feldman, et al.
American Journal of Human Genetics|April 1, 1995
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6G J Feldman, N H Robin, L A Brueton, 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.
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Succinimide hydroxamic acids as potent inhibitors of histone deacetylase (HDAC)Michael L Curtin, Robert B Garland, H Robin Heyman, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Cryobiology|November 26, 2008
Towards cryopreservation of Greenshell mussel (Perna canaliculus) oocytesSerean L Adams, H Robin Tervit, Lindsay T McGowan, et al.
Pageof 30