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L G Shaffer

Showing results (81-90 of 133) with videos related to

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Prenatal Diagnosis|September 1, 1995
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicismC Jones, C Booth, D Rita, et al.
Leukemia|September 23, 2006
A dual-color FISH assay distinguishes between ELL and MLLT1 (ENL) gene rearrangements in t(11;19)-positive acute leukemiaJ S Biggerstaff, W Liu, M L Slovak, et al.
Journal of Medical Genetics|September 9, 2000
Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayK Kosaki, R Kosaki, W P Robinson, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat geneD Li, P Burch, O Gonzalez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
American College of Medical Genetics statement of diagnostic testing for uniparental disomyL G Shaffer, N Agan, J D Goldberg, et al.
American Journal of Medical Genetics|December 11, 1996
Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16A S Schneider, F Z Bischoff, C McCaskill, et al.
American Journal of Medical Genetics|May 8, 1995
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter)A Scheuerle, J L Zenger-Hain, D L Van Dyke, et al.
American Journal of Medical Genetics. Part A|October 9, 2004
Partial trisomy of chromosome 10(q22-q24) due to maternal insertional translocation (15;10)J Y Han, K H Kim, H J Jun, et al.
American Journal of Medical Genetics|August 1, 1994
De novo proximal interstitial deletions of 14q: cytogenetic and molecular investigationsS K Shapira, K L Anderson, A Orr-Urtregar, et al.
American Journal of Medical Genetics|January 2, 1995
Duplication 3q syndrome: molecular delineation of the critical regionM S Aqua, P Rizzu, E A Lindsay, et al.
Pageof 14

Showing results (81-90 of 133) with videos related to

Sort By:
Pageof 14
Prenatal Diagnosis|September 1, 1995
Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicismC Jones, C Booth, D Rita, et al.
Leukemia|September 23, 2006
A dual-color FISH assay distinguishes between ELL and MLLT1 (ENL) gene rearrangements in t(11;19)-positive acute leukemiaJ S Biggerstaff, W Liu, M L Slovak, et al.
Journal of Medical Genetics|September 9, 2000
Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayK Kosaki, R Kosaki, W P Robinson, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat geneD Li, P Burch, O Gonzalez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
American College of Medical Genetics statement of diagnostic testing for uniparental disomyL G Shaffer, N Agan, J D Goldberg, et al.
American Journal of Medical Genetics|December 11, 1996
Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16A S Schneider, F Z Bischoff, C McCaskill, et al.
American Journal of Medical Genetics|May 8, 1995
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter)A Scheuerle, J L Zenger-Hain, D L Van Dyke, et al.
American Journal of Medical Genetics. Part A|October 9, 2004
Partial trisomy of chromosome 10(q22-q24) due to maternal insertional translocation (15;10)J Y Han, K H Kim, H J Jun, et al.
American Journal of Medical Genetics|August 1, 1994
De novo proximal interstitial deletions of 14q: cytogenetic and molecular investigationsS K Shapira, K L Anderson, A Orr-Urtregar, et al.
American Journal of Medical Genetics|January 2, 1995
Duplication 3q syndrome: molecular delineation of the critical regionM S Aqua, P Rizzu, E A Lindsay, et al.
Pageof 14