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Drug Discovery Today
|
July 12, 2008
The array CGH and its clinical applications
Marwan Shinawi, Sau Wai Cheung
American Journal of Medical Genetics. Part A
|
July 4, 2015
Refinement of the postnatal growth restriction locus of chromosome 5q12-13 deletion syndrome
J Lloyd Holder, Sau-Wai Cheung
American Journal of Medical Genetics. Part A
|
April 29, 2010
Introductory comments on special section-genomic microduplications: When adding may equal subtracting
Carlos A Bacino, Sau-Wai Cheung
Expert Review of Molecular Diagnostics
|
March 31, 2021
Noninvasive prenatal screening for fetal sex chromosome aneuploidies
Cechuan Deng, Sau Wai Cheung, Hongqian Liu
American Journal of Medical Genetics. Part A
|
April 29, 2010
Challenges in clinical interpretation of microduplications detected by array CGH analysis
Pawel Stankiewicz, Amber N Pursley, Sau Wai Cheung
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
September 4, 2009
Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting
Amy M Breman, Wei-min Bi, Sau Wai Cheung
Neurology
|
October 25, 2017
Clinical Reasoning: A common cause for Phelan-McDermid syndrome and neurofibromatosis type 2: One ring to bind them
Ariel M Lyons-Warren, Sau Wai Cheung, J Lloyd Holder
American Journal of Medical Genetics. Part A
|
June 11, 2015
A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures
Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome
J Lloyd Holder, Timothy E Lotze, Carlos Bacino, et al.
Expert Review of Molecular Diagnostics
|
November 1, 2005
Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysis
Benjamin B Roa, Joseph Pulliam, Christine M Eng, et al.
Page
of 17
Search research articles
Search
Showing results (1-10 of 165) with videos related to
Sort By:
Page
of 17
Drug Discovery Today
|
July 12, 2008
The array CGH and its clinical applications
Marwan Shinawi, Sau Wai Cheung
American Journal of Medical Genetics. Part A
|
July 4, 2015
Refinement of the postnatal growth restriction locus of chromosome 5q12-13 deletion syndrome
J Lloyd Holder, Sau-Wai Cheung
American Journal of Medical Genetics. Part A
|
April 29, 2010
Introductory comments on special section-genomic microduplications: When adding may equal subtracting
Carlos A Bacino, Sau-Wai Cheung
Expert Review of Molecular Diagnostics
|
March 31, 2021
Noninvasive prenatal screening for fetal sex chromosome aneuploidies
Cechuan Deng, Sau Wai Cheung, Hongqian Liu
American Journal of Medical Genetics. Part A
|
April 29, 2010
Challenges in clinical interpretation of microduplications detected by array CGH analysis
Pawel Stankiewicz, Amber N Pursley, Sau Wai Cheung
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
September 4, 2009
Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting
Amy M Breman, Wei-min Bi, Sau Wai Cheung
Neurology
|
October 25, 2017
Clinical Reasoning: A common cause for Phelan-McDermid syndrome and neurofibromatosis type 2: One ring to bind them
Ariel M Lyons-Warren, Sau Wai Cheung, J Lloyd Holder
American Journal of Medical Genetics. Part A
|
June 11, 2015
A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures
Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome
J Lloyd Holder, Timothy E Lotze, Carlos Bacino, et al.
Expert Review of Molecular Diagnostics
|
November 1, 2005
Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysis
Benjamin B Roa, Joseph Pulliam, Christine M Eng, et al.
Page
of 17