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Anne V Hing

Showing results (21-30 of 37) with videos related to

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Molecular Cytogenetics|May 13, 2008
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridizationKaren D Tsuchiya, Kent E Opheim, Mark C Hannibal, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 21, 2012
Evaluation of ICD-9-CM codes for craniofacial microsomiaDaniela V Luquetti, Babette S Saltzman, Daniela Vivaldi, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
IGF1R variants associated with isolated single suture craniosynostosisMichael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
American Journal of Medical Genetics. Part A|January 20, 2017
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndromeTara L Wenger, Penny Chow, Stephanie C Randle, et al.
Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 29, 2016
Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical researchCarrie L Heike, Erin Wallace, Matthew L Speltz, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosisHeather C Mefford, Neil Shafer, Francesca Antonacci, et al.
American Journal of Human Genetics|August 9, 2014
Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosisJoshua D Smith, Anne V Hing, Christine M Clarke, et al.
American Journal of Medical Genetics. Part A|March 9, 2007
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutationsMarianne L Seto, Anne V Hing, Jocelyn Chang, et al.
American Journal of Medical Genetics. Part A|July 22, 2021
Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequenceTara L Wenger, Jonathan Perkins, Julia Parish-Morris, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Molecular Cytogenetics|May 13, 2008
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridizationKaren D Tsuchiya, Kent E Opheim, Mark C Hannibal, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 21, 2012
Evaluation of ICD-9-CM codes for craniofacial microsomiaDaniela V Luquetti, Babette S Saltzman, Daniela Vivaldi, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
IGF1R variants associated with isolated single suture craniosynostosisMichael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
American Journal of Medical Genetics. Part A|January 20, 2017
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndromeTara L Wenger, Penny Chow, Stephanie C Randle, et al.
Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 29, 2016
Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical researchCarrie L Heike, Erin Wallace, Matthew L Speltz, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosisHeather C Mefford, Neil Shafer, Francesca Antonacci, et al.
American Journal of Human Genetics|August 9, 2014
Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosisJoshua D Smith, Anne V Hing, Christine M Clarke, et al.
American Journal of Medical Genetics. Part A|March 9, 2007
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutationsMarianne L Seto, Anne V Hing, Jocelyn Chang, et al.
American Journal of Medical Genetics. Part A|July 22, 2021
Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequenceTara L Wenger, Jonathan Perkins, Julia Parish-Morris, et al.
Pageof 4