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R A Schultz

Showing results (101-110 of 107) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 8, 2015
Diagnostic utility of microarray testing in pregnancy lossJ A Rosenfeld, M E Tucker, L F Escobar, et al.
Leukemia|March 9, 2011
Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemiaL Yu, M L Slovak, K Mannoor, et al.
Basic Life Sciences|January 1, 1986
Molecular approaches to the study of nucleotide excision repair in eukaryotesE C Friedberg, D P Barbis, J M Chenevert, et al.
Cell|August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHK A Henning, L Li, N Iyer, et al.
Cytogenetic and Genome Research|September 10, 2009
Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agentsA W Hemphill, Y Akkari, A H Newell, et al.
Molecular Syndromology|November 1, 2012
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 MicrodeletionsR N Traylor, W B Dobyns, J A Rosenfeld, et al.
Molecular Syndromology|April 20, 2013
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and MicrocephalyJ A Rosenfeld, K H Kim, B Angle, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 8, 2015
Diagnostic utility of microarray testing in pregnancy lossJ A Rosenfeld, M E Tucker, L F Escobar, et al.
Leukemia|March 9, 2011
Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemiaL Yu, M L Slovak, K Mannoor, et al.
Basic Life Sciences|January 1, 1986
Molecular approaches to the study of nucleotide excision repair in eukaryotesE C Friedberg, D P Barbis, J M Chenevert, et al.
Cell|August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHK A Henning, L Li, N Iyer, et al.
Cytogenetic and Genome Research|September 10, 2009
Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agentsA W Hemphill, Y Akkari, A H Newell, et al.
Molecular Syndromology|November 1, 2012
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 MicrodeletionsR N Traylor, W B Dobyns, J A Rosenfeld, et al.
Molecular Syndromology|April 20, 2013
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and MicrocephalyJ A Rosenfeld, K H Kim, B Angle, et al.
Pageof 11