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Sau W Cheung

Showing results (11-20 of 33) with videos related to

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American Journal of Hematology|December 29, 2007
Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemiaAnkita Patel, Sung-Hae Kang, Patrick Alan Lennon, et al.
American Journal of Perinatology|August 18, 2016
Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal KaryotypeEran Bornstein, Sharon Berger, Sau W Cheung, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNAZöe Powis, Sung-Hae L Kang, M Lance Cooper, et al.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 19, 2005
Development and validation of a CGH microarray for clinical cytogenetic diagnosisSau W Cheung, Chad A Shaw, Wei Yu, et al.
Human Genetics|June 23, 2006
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocationsZhishuo Ou, Małgorzata Jarmuz, Steven P Sparagana, et al.
American Journal of Human Genetics|January 9, 2008
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndromeShay Ben-Shachar, Zhishuo Ou, Chad A Shaw, et al.
Human Mutation|September 9, 2020
Cytogenetically visible inversions are formed by multiple molecular mechanismsMaria Pettersson, Christopher M Grochowski, Josephine Wincent, et al.
Pediatrics|December 3, 2008
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysisXin-Yan Lu, Mai T Phung, Chad A Shaw, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
American Journal of Hematology|December 29, 2007
Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemiaAnkita Patel, Sung-Hae Kang, Patrick Alan Lennon, et al.
American Journal of Perinatology|August 18, 2016
Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal KaryotypeEran Bornstein, Sharon Berger, Sau W Cheung, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNAZöe Powis, Sung-Hae L Kang, M Lance Cooper, et al.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 19, 2005
Development and validation of a CGH microarray for clinical cytogenetic diagnosisSau W Cheung, Chad A Shaw, Wei Yu, et al.
Human Genetics|June 23, 2006
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocationsZhishuo Ou, Małgorzata Jarmuz, Steven P Sparagana, et al.
American Journal of Human Genetics|January 9, 2008
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndromeShay Ben-Shachar, Zhishuo Ou, Chad A Shaw, et al.
Human Mutation|September 9, 2020
Cytogenetically visible inversions are formed by multiple molecular mechanismsMaria Pettersson, Christopher M Grochowski, Josephine Wincent, et al.
Pediatrics|December 3, 2008
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysisXin-Yan Lu, Mai T Phung, Chad A Shaw, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Pageof 4