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Stuart Schwartz

Showing results (11-20 of 73) with videos related to

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American Journal of Medical Genetics. Part A|April 27, 2004
Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotypeCathy Chu, Stuart Schwartz, Elizabeth McPherson
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|July 27, 2012
Fatal Henoch-Schönlein purpura in an adult with Dieulafoy lesionsDan A Cristescu, Candice Yuvienco, Stuart Schwartz
American Journal of Medical Genetics. Part A|April 14, 2007
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndromeMelissa A Dempsey, Stuart Schwartz, Darrel J Waggoner
Prenatal Diagnosis|September 5, 2002
Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screeningMichael D Graf, Prabhcharan Gill, Michael Krew, et al.
Cancer Research|May 31, 2002
Chemotherapy-induced O(6)-benzylguanine-resistant alkyltransferase mutations in mismatch-deficient colon cancerLili Liu, Stuart Schwartz, Brian M Davis, et al.
Cytogenetic and Genome Research|November 18, 2014
Four-copy number intervals in SNP microarray analysis: unique patterns and positionsPeter R Papenhausen, Carla A Kelly, Val Zvereff, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2024
Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomesAlexandra Arreola, Gloria Haskell, Inder Gadi, et al.
Molecular and Cellular Biology|October 16, 2003
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lagM Katharine Rudd, Robert W Mays, Stuart Schwartz, et al.
Cancer Genetics and Cytogenetics|August 26, 2003
Analysis of microsatellite instability and X-inactivation in ovarian borderline tumors lacking numerical abnormalities by comparative genomic hybridizationNancy G Wolf, Carol Farver, Fadi W Abdul-Karim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Prader-Willi syndromeSuzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|April 27, 2004
Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotypeCathy Chu, Stuart Schwartz, Elizabeth McPherson
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|July 27, 2012
Fatal Henoch-Schönlein purpura in an adult with Dieulafoy lesionsDan A Cristescu, Candice Yuvienco, Stuart Schwartz
American Journal of Medical Genetics. Part A|April 14, 2007
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndromeMelissa A Dempsey, Stuart Schwartz, Darrel J Waggoner
Prenatal Diagnosis|September 5, 2002
Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screeningMichael D Graf, Prabhcharan Gill, Michael Krew, et al.
Cancer Research|May 31, 2002
Chemotherapy-induced O(6)-benzylguanine-resistant alkyltransferase mutations in mismatch-deficient colon cancerLili Liu, Stuart Schwartz, Brian M Davis, et al.
Cytogenetic and Genome Research|November 18, 2014
Four-copy number intervals in SNP microarray analysis: unique patterns and positionsPeter R Papenhausen, Carla A Kelly, Val Zvereff, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2024
Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomesAlexandra Arreola, Gloria Haskell, Inder Gadi, et al.
Molecular and Cellular Biology|October 16, 2003
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lagM Katharine Rudd, Robert W Mays, Stuart Schwartz, et al.
Cancer Genetics and Cytogenetics|August 26, 2003
Analysis of microsatellite instability and X-inactivation in ovarian borderline tumors lacking numerical abnormalities by comparative genomic hybridizationNancy G Wolf, Carol Farver, Fadi W Abdul-Karim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Prader-Willi syndromeSuzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, et al.
Pageof 8