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Lisa G Shaffer

Showing results (31-40 of 215) with videos related to

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Prenatal Diagnosis|March 5, 2011
Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 3, 2014
Narrowing the localization of the region breakpoint in most frequent Robertsonian translocationsMalgorzata Jarmuz-Szymczak, Joanna Janiszewska, Krzysztof Szyfter, et al.
American Journal of Medical Genetics|September 5, 2002
Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocationsSue Ann Berend, Bassem A Bejjani, Christopher McCaskill, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 6, 2004
Trisomy 14 mosaicism: a case report and review of the literatureM Fran Lynch, Caraciolo J Fernandes, Lisa G Shaffer, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Prenatal Diagnosis of Charcot-Marie-Tooth Disease Type 1ACatherine D Kashork, Ken-Shiung Chen, James R Lupski, et al.
Human Genetics|July 21, 2021
Identification of aneuploidy in dogs screened by a SNP microarrayLisa G Shaffer, Bradley Hopp, Marek Switonski, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardationEmily Chen, Elise Obolensky, Katherine A Rauen, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
From VACTERL-H to heterotaxy: variable expressivity of ZIC3-related disordersBrian Chung, Lisa G Shaffer, Sarah Keating, et al.
American Journal of Human Genetics|February 3, 2007
The Evolution of satellite III DNA subfamilies among primatesMalgorzata Jarmuz, Caron D Glotzbach, Kristen A Bailey, et al.
Pageof 22

Showing results (31-40 of 215) with videos related to

Sort By:
Pageof 22
Prenatal Diagnosis|March 5, 2011
Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 3, 2014
Narrowing the localization of the region breakpoint in most frequent Robertsonian translocationsMalgorzata Jarmuz-Szymczak, Joanna Janiszewska, Krzysztof Szyfter, et al.
American Journal of Medical Genetics|September 5, 2002
Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocationsSue Ann Berend, Bassem A Bejjani, Christopher McCaskill, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 6, 2004
Trisomy 14 mosaicism: a case report and review of the literatureM Fran Lynch, Caraciolo J Fernandes, Lisa G Shaffer, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Prenatal Diagnosis of Charcot-Marie-Tooth Disease Type 1ACatherine D Kashork, Ken-Shiung Chen, James R Lupski, et al.
Human Genetics|July 21, 2021
Identification of aneuploidy in dogs screened by a SNP microarrayLisa G Shaffer, Bradley Hopp, Marek Switonski, et al.
American Journal of Medical Genetics. Part A|October 17, 2008
Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardationEmily Chen, Elise Obolensky, Katherine A Rauen, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
From VACTERL-H to heterotaxy: variable expressivity of ZIC3-related disordersBrian Chung, Lisa G Shaffer, Sarah Keating, et al.
American Journal of Human Genetics|February 3, 2007
The Evolution of satellite III DNA subfamilies among primatesMalgorzata Jarmuz, Caron D Glotzbach, Kristen A Bailey, et al.
Pageof 22