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Sau W Cheung

Showing results (1-10 of 33) with videos related to

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Expert Review of Molecular Diagnostics|June 1, 2018
Novel applications of array comparative genomic hybridization in molecular diagnosticsSau W Cheung, Weimin Bi
Methods in Molecular Biology (Clifton, N.J.)|November 29, 2015
Application of DNA Microarray to Clinical DiagnosticsAnkita Patel, Sau W Cheung
The New England Journal of Medicine|April 2, 2015
Accurate description of DNA-based noninvasive prenatal screeningSau W Cheung, Ankita Patel, Tak Y Leung
Prenatal Diagnosis|December 15, 2005
Prenatal diagnosis of PLP1 copy number by array comparative genomic hybridizationJennifer A Lee, Sau W Cheung, Patricia A Ward, et al.
Prenatal Diagnosis|August 30, 2018
Microarray analysis: First-trimester maternal serum free β-hCG and the risk of significant copy number variantsEran Bornstein, Moti Gulersen, David Krantz, et al.
Critical Reviews in Clinical Laboratory Sciences|June 1, 2014
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics eraYong-Hui Jiang, Yi Wang, Xu Xiu, et al.
Human Molecular Genetics|June 16, 2006
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher diseaseJennifer A Lee, Ken Inoue, Sau W Cheung, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14Lindsay C Burrage, Tanya N Eble, Patricia M Hixson, et al.
American Journal of Medical Genetics. Part A|July 31, 2008
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangementZhishuo Ou, Donna M Martin, Jirair K Bedoyan, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently "balanced" paracentric inversion of 14(q21q23)Yong-Hui Jiang, Jose E Martinez, Zhishuo Ou, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Expert Review of Molecular Diagnostics|June 1, 2018
Novel applications of array comparative genomic hybridization in molecular diagnosticsSau W Cheung, Weimin Bi
Methods in Molecular Biology (Clifton, N.J.)|November 29, 2015
Application of DNA Microarray to Clinical DiagnosticsAnkita Patel, Sau W Cheung
The New England Journal of Medicine|April 2, 2015
Accurate description of DNA-based noninvasive prenatal screeningSau W Cheung, Ankita Patel, Tak Y Leung
Prenatal Diagnosis|December 15, 2005
Prenatal diagnosis of PLP1 copy number by array comparative genomic hybridizationJennifer A Lee, Sau W Cheung, Patricia A Ward, et al.
Prenatal Diagnosis|August 30, 2018
Microarray analysis: First-trimester maternal serum free β-hCG and the risk of significant copy number variantsEran Bornstein, Moti Gulersen, David Krantz, et al.
Critical Reviews in Clinical Laboratory Sciences|June 1, 2014
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics eraYong-Hui Jiang, Yi Wang, Xu Xiu, et al.
Human Molecular Genetics|June 16, 2006
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher diseaseJennifer A Lee, Ken Inoue, Sau W Cheung, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14Lindsay C Burrage, Tanya N Eble, Patricia M Hixson, et al.
American Journal of Medical Genetics. Part A|July 31, 2008
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangementZhishuo Ou, Donna M Martin, Jirair K Bedoyan, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently "balanced" paracentric inversion of 14(q21q23)Yong-Hui Jiang, Jose E Martinez, Zhishuo Ou, et al.
Pageof 4