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Arthur R Brothman

Showing results (31-40 of 45) with videos related to

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Genes, Chromosomes & Cancer|August 3, 2005
Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGHRebecca R Selzer, Todd A Richmond, Nathan J Pofahl, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?Cynthia J Curry, Rong Mao, Emily Aston, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Craniorachischisis and omphalocele in a stillborn cynomolgus monkey (Macaca fascicularis)Charleen M Moore, Edward J Dick, Gene B Hubbard, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardationAnnika M Svensson, Cynthia J Curry, Sarah T South, et al.
Cell Cycle (Georgetown, Tex.)|December 9, 2014
Immortalization of normal human mammary epithelial cells in two steps by direct targeting of senescence barriers does not require gross genomic alterationsJames C Garbe, Lukas Vrba, Klara Sputova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2003
Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected]James T Mascarello, Linda D Cooley, Keri Davison, et al.
Archives of Pathology & Laboratory Medicine|November 29, 2002
Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probesJames T Mascarello, Arthur R Brothman, Keri Davison, et al.
Archives of Pathology & Laboratory Medicine|July 13, 2006
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for yearsArthur R Brothman, Nancy R Schneider, Irene Saikevych, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 12, 2009
Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratoriesKaren D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2011
College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysisArthur R Brothman, Michelle M Dolan, Barbara K Goodman, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Genes, Chromosomes & Cancer|August 3, 2005
Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGHRebecca R Selzer, Todd A Richmond, Nathan J Pofahl, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?Cynthia J Curry, Rong Mao, Emily Aston, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Craniorachischisis and omphalocele in a stillborn cynomolgus monkey (Macaca fascicularis)Charleen M Moore, Edward J Dick, Gene B Hubbard, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardationAnnika M Svensson, Cynthia J Curry, Sarah T South, et al.
Cell Cycle (Georgetown, Tex.)|December 9, 2014
Immortalization of normal human mammary epithelial cells in two steps by direct targeting of senescence barriers does not require gross genomic alterationsJames C Garbe, Lukas Vrba, Klara Sputova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2003
Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected]James T Mascarello, Linda D Cooley, Keri Davison, et al.
Archives of Pathology & Laboratory Medicine|November 29, 2002
Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probesJames T Mascarello, Arthur R Brothman, Keri Davison, et al.
Archives of Pathology & Laboratory Medicine|July 13, 2006
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for yearsArthur R Brothman, Nancy R Schneider, Irene Saikevych, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 12, 2009
Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratoriesKaren D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2011
College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysisArthur R Brothman, Michelle M Dolan, Barbara K Goodman, et al.
Pageof 5