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Expert Review of Molecular Diagnostics
|
June 1, 2018
Novel applications of array comparative genomic hybridization in molecular diagnostics
Sau W Cheung, Weimin Bi
American Journal of Human Genetics
|
February 3, 2007
Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike
Jiong Yan, Weimin Bi, James R Lupski
American Journal of Human Genetics
|
October 11, 2002
Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2
Christine J Shaw, Weimin Bi, James R Lupski
American Journal of Medical Genetics. Part A
|
May 14, 2026
De Novo 2.2 Mb 19q13.42-q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model
Amanda Toledo, Sarah Araji, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2011
A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)
Luis A Umaña, Pilar Magoulas, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2016
4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions
Weimin Bi, Sau-Wai Cheung, Amy M Breman, et al.
The Journal of Clinical Investigation
|
October 7, 2006
Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)
Katherina Walz, Richard Paylor, Jiong Yan, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2016
Novel EED mutation in patient with Weaver syndrome
Erin Cooney, Weimin Bi, Alan E Schlesinger, et al.
Chinese Medical Journal
|
July 23, 2002
Detection of occult metastases in lymph nodes from patients with colorectal carcinoma by reverse transcriptase-polymerase chain reaction
Zhongmin Liu, Xin Ye, Weimin Bi, et al.
Current Protocols in Human Genetics
|
March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions
Qian Liu, Christopher M Grochowski, Weimin Bi, et al.
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of 14
Search research articles
Search
Showing results (1-10 of 138) with videos related to
Sort By:
Page
of 14
Expert Review of Molecular Diagnostics
|
June 1, 2018
Novel applications of array comparative genomic hybridization in molecular diagnostics
Sau W Cheung, Weimin Bi
American Journal of Human Genetics
|
February 3, 2007
Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike
Jiong Yan, Weimin Bi, James R Lupski
American Journal of Human Genetics
|
October 11, 2002
Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2
Christine J Shaw, Weimin Bi, James R Lupski
American Journal of Medical Genetics. Part A
|
May 14, 2026
De Novo 2.2 Mb 19q13.42-q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model
Amanda Toledo, Sarah Araji, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2011
A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)
Luis A Umaña, Pilar Magoulas, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2016
4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions
Weimin Bi, Sau-Wai Cheung, Amy M Breman, et al.
The Journal of Clinical Investigation
|
October 7, 2006
Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)
Katherina Walz, Richard Paylor, Jiong Yan, et al.
American Journal of Medical Genetics. Part A
|
November 22, 2016
Novel EED mutation in patient with Weaver syndrome
Erin Cooney, Weimin Bi, Alan E Schlesinger, et al.
Chinese Medical Journal
|
July 23, 2002
Detection of occult metastases in lymph nodes from patients with colorectal carcinoma by reverse transcriptase-polymerase chain reaction
Zhongmin Liu, Xin Ye, Weimin Bi, et al.
Current Protocols in Human Genetics
|
March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions
Qian Liu, Christopher M Grochowski, Weimin Bi, et al.
Page
of 14