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

Arthur R Brothman

Showing results (1-10 of 45) with videos related to

Pageof 5
Sort By:
American Journal of Medical Genetics|October 31, 2002
Cytogenetics and molecular genetics of cancer of the prostateArthur R Brothman
Methods in Enzymology|November 7, 2002
Methylation in gene promoters: assessment after laser capture microdissectionArthur R Brothman, Jiang Cui
Cancer Genetics|April 21, 2011
Cytogenomic aberrations associated with prostate cancerGuangyu Gu, Arthur R Brothman
Nature Genetics|September 5, 2007
Copy number variations and clinical cytogenetic diagnosis of constitutional disordersCharles Lee, A John Iafrate, Arthur R Brothman
Clinical Obstetrics and Gynecology|February 28, 2008
Genomic medicine in prenatal diagnosisSarah T South, Zhong Chen, Arthur R Brothman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delayJennifer Saam, Jim Gudgeon, Emily Aston, et al.
Prenatal Diagnosis|November 10, 2012
Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assayChristian N Paxton, Arthur R Brothman, Katherine B Geiersbach
Cancer Genetics and Cytogenetics|July 18, 2006
Unexpected cytogenetic finding in acute lymphoblastic leukemia: a case of del(5q) with a cryptic t(12;21)Sarah T South, J Kimble Frazer, Arthur R Brothman, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Paternal uniparental disomy of chromosome 14: confirmation of a clinically-recognizable phenotypeDavid A Stevenson, Arthur R Brothman, Zhong Chen, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocationsSarah T South, Heidi Whitby, Agatino Battaglia, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|October 31, 2002
Cytogenetics and molecular genetics of cancer of the prostateArthur R Brothman
Methods in Enzymology|November 7, 2002
Methylation in gene promoters: assessment after laser capture microdissectionArthur R Brothman, Jiang Cui
Cancer Genetics|April 21, 2011
Cytogenomic aberrations associated with prostate cancerGuangyu Gu, Arthur R Brothman
Nature Genetics|September 5, 2007
Copy number variations and clinical cytogenetic diagnosis of constitutional disordersCharles Lee, A John Iafrate, Arthur R Brothman
Clinical Obstetrics and Gynecology|February 28, 2008
Genomic medicine in prenatal diagnosisSarah T South, Zhong Chen, Arthur R Brothman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delayJennifer Saam, Jim Gudgeon, Emily Aston, et al.
Prenatal Diagnosis|November 10, 2012
Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assayChristian N Paxton, Arthur R Brothman, Katherine B Geiersbach
Cancer Genetics and Cytogenetics|July 18, 2006
Unexpected cytogenetic finding in acute lymphoblastic leukemia: a case of del(5q) with a cryptic t(12;21)Sarah T South, J Kimble Frazer, Arthur R Brothman, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Paternal uniparental disomy of chromosome 14: confirmation of a clinically-recognizable phenotypeDavid A Stevenson, Arthur R Brothman, Zhong Chen, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocationsSarah T South, Heidi Whitby, Agatino Battaglia, et al.
Pageof 5