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Blake C Ballif

Showing results (21-30 of 83) with videos related to

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Molecular Cytogenetics|August 12, 2009
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case reportRyan N Traylor, Zheng Fan, Beth Hudson, et al.
Journal of Neurodevelopmental Disorders|July 7, 2011
Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplicationsJill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, et al.
Cytogenetic and Genome Research|February 9, 2018
An International Genetic Survey of Breed-Specific Diseases in Working Dogs from the United States, Israel, and PolandLisa G Shaffer, Christina J Ramirez, Patricia Phelps, et al.
Human Genetics|August 9, 2021
The PMEL gene and merle (dapple) in the dachshund: cryptic, hidden, and mosaic variants demonstrate the need for genetic testing prior to breedingBlake C Ballif, Lisa J Emerson, Christina J Ramirez, et al.
American Journal of Medical Genetics. Part A|July 17, 2007
The clinical utility of enhanced subtelomeric coverage in array CGHBlake C Ballif, Scott G Sulpizio, Richard M Lloyd, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?Bassem A Bejjani, Reza Saleki, Blake C Ballif, et al.
Human Genetics|January 13, 2010
Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPEJill A Rosenfeld, Blake C Ballif, Donna M Martin, et al.
Cytogenetic and Genome Research|August 3, 2018
The PMEL Gene and Merle in the Domestic Dog: A Continuum of Insertion Lengths Leads to a Spectrum of Coat Color Variations in Australian Shepherds and Related BreedsBlake C Ballif, Christina J Ramirez, Casey R Carl, et al.
Human Genetics|November 15, 2018
Standards and guidelines for canine clinical genetic testing laboratoriesLisa G Shaffer, Kyle Sundin, Anja Geretschlaeger, et al.
Plos One|August 12, 2009
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndromeJill A Rosenfeld, Blake C Ballif, Ann Lucas, et al.
Pageof 9

Showing results (21-30 of 83) with videos related to

Sort By:
Pageof 9
Molecular Cytogenetics|August 12, 2009
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case reportRyan N Traylor, Zheng Fan, Beth Hudson, et al.
Journal of Neurodevelopmental Disorders|July 7, 2011
Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplicationsJill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, et al.
Cytogenetic and Genome Research|February 9, 2018
An International Genetic Survey of Breed-Specific Diseases in Working Dogs from the United States, Israel, and PolandLisa G Shaffer, Christina J Ramirez, Patricia Phelps, et al.
Human Genetics|August 9, 2021
The PMEL gene and merle (dapple) in the dachshund: cryptic, hidden, and mosaic variants demonstrate the need for genetic testing prior to breedingBlake C Ballif, Lisa J Emerson, Christina J Ramirez, et al.
American Journal of Medical Genetics. Part A|July 17, 2007
The clinical utility of enhanced subtelomeric coverage in array CGHBlake C Ballif, Scott G Sulpizio, Richard M Lloyd, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?Bassem A Bejjani, Reza Saleki, Blake C Ballif, et al.
Human Genetics|January 13, 2010
Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPEJill A Rosenfeld, Blake C Ballif, Donna M Martin, et al.
Cytogenetic and Genome Research|August 3, 2018
The PMEL Gene and Merle in the Domestic Dog: A Continuum of Insertion Lengths Leads to a Spectrum of Coat Color Variations in Australian Shepherds and Related BreedsBlake C Ballif, Christina J Ramirez, Casey R Carl, et al.
Human Genetics|November 15, 2018
Standards and guidelines for canine clinical genetic testing laboratoriesLisa G Shaffer, Kyle Sundin, Anja Geretschlaeger, et al.
Plos One|August 12, 2009
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndromeJill A Rosenfeld, Blake C Ballif, Ann Lucas, et al.
Pageof 9