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Barbara R Pober

Showing results (31-40 of 57) with videos related to

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Journal of Autism and Developmental Disorders|November 23, 2017
Brief Report: Major Depressive Disorder with Psychotic Features in Williams Syndrome: A Case SeriesFrancisca Valdes, Christopher J Keary, Jennifer E Mullett, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangementPeining Li, Hui Z Zhang, Shannon Huff, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 16, 2010
Maternal periconceptional exposure to cigarette smoking and alcohol consumption and congenital diaphragmatic herniaKristin M Caspers, Cristiana Oltean, Paul A Romitti, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Multisystem study of 20 older adults with Williams syndromeElizabeth M Cherniske, Thomas O Carpenter, Cheryl Klaiman, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic herniaKanwal Qidwai, David M Pearson, Gayle Simpson Patel, et al.
American Journal of Medical Genetics. Part A|June 13, 2014
Skin findings in Williams syndromeBeth A Kozel, Susan J Bayliss, David R Berk, et al.
American Journal of Medical Genetics. Part A|February 21, 2020
Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndromeMichael Lugo, Zoë C Wong, Charles J Billington, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 16, 2013
Rapamycin inhibits smooth muscle cell proliferation and obstructive arteriopathy attributable to elastin deficiencyWei Li, Qingle Li, Lingfeng Qin, et al.
Journal of Autism and Developmental Disorders|April 10, 2021
Repetitive Thoughts and Repetitive Behaviors in Williams SyndromeJohn C Huston, Robyn P Thom, Caitlin T Ravichandran, et al.
Journal of Genetic Counseling|February 4, 2012
Genetic counseling as a tool for type 2 diabetes prevention: a genetic counseling framework for common polygenetic disordersJessica L Waxler, Kelsey E O'Brien, Linda M Delahanty, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Journal of Autism and Developmental Disorders|November 23, 2017
Brief Report: Major Depressive Disorder with Psychotic Features in Williams Syndrome: A Case SeriesFrancisca Valdes, Christopher J Keary, Jennifer E Mullett, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangementPeining Li, Hui Z Zhang, Shannon Huff, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 16, 2010
Maternal periconceptional exposure to cigarette smoking and alcohol consumption and congenital diaphragmatic herniaKristin M Caspers, Cristiana Oltean, Paul A Romitti, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Multisystem study of 20 older adults with Williams syndromeElizabeth M Cherniske, Thomas O Carpenter, Cheryl Klaiman, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic herniaKanwal Qidwai, David M Pearson, Gayle Simpson Patel, et al.
American Journal of Medical Genetics. Part A|June 13, 2014
Skin findings in Williams syndromeBeth A Kozel, Susan J Bayliss, David R Berk, et al.
American Journal of Medical Genetics. Part A|February 21, 2020
Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndromeMichael Lugo, Zoë C Wong, Charles J Billington, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 16, 2013
Rapamycin inhibits smooth muscle cell proliferation and obstructive arteriopathy attributable to elastin deficiencyWei Li, Qingle Li, Lingfeng Qin, et al.
Journal of Autism and Developmental Disorders|April 10, 2021
Repetitive Thoughts and Repetitive Behaviors in Williams SyndromeJohn C Huston, Robyn P Thom, Caitlin T Ravichandran, et al.
Journal of Genetic Counseling|February 4, 2012
Genetic counseling as a tool for type 2 diabetes prevention: a genetic counseling framework for common polygenetic disordersJessica L Waxler, Kelsey E O'Brien, Linda M Delahanty, et al.
Pageof 6