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Lisa G Shaffer

Showing results (91-100 of 215) with videos related to

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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.
Human Genetics|March 10, 2009
Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangementsCarla S D'Angelo, Marzena Gajecka, Chong A Kim, et al.
BMC Genomics|January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionYong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Prenatal Diagnosis|January 3, 2014
In case you missed it: the Prenatal Diagnosis section editors bring you the most significant advances of 2013Diana W Bianchi, Tim Van Mieghem, Lisa G Shaffer, 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.
The Korean Journal of Laboratory Medicine|July 7, 2010
A rare case of acute lymphoblastic leukemia with t(12;17)(p13;q21)Ji Eun Kim, Kwang Sook Woo, Kyung Eun Kim, 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.
Prenatal Diagnosis|October 29, 2009
Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotypeLinda Kleeman, Diana W Bianchi, Lisa G Shaffer, et al.
Pageof 22

Showing results (91-100 of 215) with videos related to

Sort By:
Pageof 22
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.
Human Genetics|March 10, 2009
Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangementsCarla S D'Angelo, Marzena Gajecka, Chong A Kim, et al.
BMC Genomics|January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionYong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Prenatal Diagnosis|January 3, 2014
In case you missed it: the Prenatal Diagnosis section editors bring you the most significant advances of 2013Diana W Bianchi, Tim Van Mieghem, Lisa G Shaffer, 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.
The Korean Journal of Laboratory Medicine|July 7, 2010
A rare case of acute lymphoblastic leukemia with t(12;17)(p13;q21)Ji Eun Kim, Kwang Sook Woo, Kyung Eun Kim, 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.
Prenatal Diagnosis|October 29, 2009
Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotypeLinda Kleeman, Diana W Bianchi, Lisa G Shaffer, et al.
Pageof 22