Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lisa G Shaffer

Showing results (141-150 of 215) with videos related to

Pageof 22
Sort By:
Cancer Genetics|December 28, 2011
Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromesKathryn A Kolquist, Roger A Schultz, Aubry Furrow, et al.
Human Genetics|August 26, 2003
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)V Reid Sutton, William H McAlister, Terry K Bertin, et al.
Prenatal Diagnosis|August 1, 2012
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundLisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyriaPhilip F Giampietro, Deepti Babu, Monica A Koehn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2011
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problemsTrilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, et al.
Prenatal Diagnosis|August 7, 2012
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnanciesLisa G Shaffer, Mindy P Dabell, Allan J Fisher, et al.
Genome Research|May 9, 2002
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouseWeimin Bi, Jiong Yan, Pawe Stankiewicz, et al.
American Journal of Human Genetics|October 14, 2014
Molecular convergence of neurodevelopmental disordersElizabeth S Chen, Carolina O Gigek, Jill A Rosenfeld, et al.
European Journal of Human Genetics : EJHG|July 1, 2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeAngela L Duker, Blake C Ballif, Erawati V Bawle, et al.
Human Molecular Genetics|August 14, 2003
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletionsWei Yu, Blake C Ballif, Catherine D Kashork, et al.
Pageof 22

Showing results (141-150 of 215) with videos related to

Sort By:
Pageof 22
Cancer Genetics|December 28, 2011
Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromesKathryn A Kolquist, Roger A Schultz, Aubry Furrow, et al.
Human Genetics|August 26, 2003
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)V Reid Sutton, William H McAlister, Terry K Bertin, et al.
Prenatal Diagnosis|August 1, 2012
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundLisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyriaPhilip F Giampietro, Deepti Babu, Monica A Koehn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2011
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problemsTrilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, et al.
Prenatal Diagnosis|August 7, 2012
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnanciesLisa G Shaffer, Mindy P Dabell, Allan J Fisher, et al.
Genome Research|May 9, 2002
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouseWeimin Bi, Jiong Yan, Pawe Stankiewicz, et al.
American Journal of Human Genetics|October 14, 2014
Molecular convergence of neurodevelopmental disordersElizabeth S Chen, Carolina O Gigek, Jill A Rosenfeld, et al.
European Journal of Human Genetics : EJHG|July 1, 2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeAngela L Duker, Blake C Ballif, Erawati V Bawle, et al.
Human Molecular Genetics|August 14, 2003
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletionsWei Yu, Blake C Ballif, Catherine D Kashork, et al.
Pageof 22