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Lisa G Shaffer

Showing results (111-120 of 215) with videos related to

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Human Genetics|August 18, 2021
Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variantChris Rorden, Marilee C Griswold, Nan Moses, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Cytogenetic analysis of obsessive-compulsive disorder (OCD): identification of a FRAXE fragile siteQing Wang, Yanghong Gu, James M Ferguson, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Plos Genetics|February 6, 2014
Large inverted duplications in the human genome form via a fold-back mechanismKaren E Hermetz, Scott Newman, Karen N Conneely, et al.
American Journal of Medical Genetics. Part A|February 9, 2010
Potocki-Shaffer syndrome: comprehensive clinical assessment, review of the literature, and proposals for medical managementDaniel T Swarr, Douglas Bloom, Richard Alan Lewis, et al.
Annals of Laboratory Medicine|July 11, 2012
A case of near-triploidy in myelodysplastic syndrome with del(5q) combined with del(1p) and del(13q)Bo-Ram Kim, Ji-Eun Kim, Kwang-Sook Woo, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpointsMarzena Gajecka, Sulagna C Saitta, Andrew J Gentles, et al.
Prenatal Diagnosis|November 9, 2002
Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysisCatherine D Kashork, V Reid Sutton, Jill S Fonda Allen, et al.
Pageof 22

Showing results (111-120 of 215) with videos related to

Sort By:
Pageof 22
Human Genetics|August 18, 2021
Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variantChris Rorden, Marilee C Griswold, Nan Moses, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Cytogenetic analysis of obsessive-compulsive disorder (OCD): identification of a FRAXE fragile siteQing Wang, Yanghong Gu, James M Ferguson, et al.
American Journal of Human Genetics|March 22, 2003
Genome architecture catalyzes nonrecurrent chromosomal rearrangementsPaweł Stankiewicz, Christine J Shaw, Jason D Dapper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Plos Genetics|February 6, 2014
Large inverted duplications in the human genome form via a fold-back mechanismKaren E Hermetz, Scott Newman, Karen N Conneely, et al.
American Journal of Medical Genetics. Part A|February 9, 2010
Potocki-Shaffer syndrome: comprehensive clinical assessment, review of the literature, and proposals for medical managementDaniel T Swarr, Douglas Bloom, Richard Alan Lewis, et al.
Annals of Laboratory Medicine|July 11, 2012
A case of near-triploidy in myelodysplastic syndrome with del(5q) combined with del(1p) and del(13q)Bo-Ram Kim, Ji-Eun Kim, Kwang-Sook Woo, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpointsMarzena Gajecka, Sulagna C Saitta, Andrew J Gentles, et al.
Prenatal Diagnosis|November 9, 2002
Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysisCatherine D Kashork, V Reid Sutton, Jill S Fonda Allen, et al.
Pageof 22