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Weimin Bi

Showing results (41-50 of 138) with videos related to

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The Journal of Molecular Diagnostics : JMD|March 28, 2009
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNASvetlana A Yatsenko, Chad A Shaw, Zhishuo Ou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Molecular Genetics & Genomic Medicine|September 29, 2021
Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patientsLei Wang, Pengfei Liu, Weimin Bi, et al.
Human Molecular Genetics|May 23, 2007
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypesWeimin Bi, Jiong Yan, Xin Shi, et al.
Genome Research|May 9, 2002
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouseWeimin Bi, Jiong Yan, Pawe Stankiewicz, 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.
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalitiesMagalie S Leduc, Zhiyv Niu, Weimin Bi, et al.
Journal of Medical Genetics|October 9, 2012
Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWeimin Bi, Frank J Probst, Joanna Wiszniewska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2012
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?Weimin Bi, Caroline Borgan, Amber N Pursley, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNASvetlana A Yatsenko, Chad A Shaw, Zhishuo Ou, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Molecular Genetics & Genomic Medicine|September 29, 2021
Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patientsLei Wang, Pengfei Liu, Weimin Bi, et al.
Human Molecular Genetics|May 23, 2007
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypesWeimin Bi, Jiong Yan, Xin Shi, et al.
Genome Research|May 9, 2002
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouseWeimin Bi, Jiong Yan, Pawe Stankiewicz, 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.
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalitiesMagalie S Leduc, Zhiyv Niu, Weimin Bi, et al.
Journal of Medical Genetics|October 9, 2012
Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWeimin Bi, Frank J Probst, Joanna Wiszniewska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2012
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?Weimin Bi, Caroline Borgan, Amber N Pursley, et al.
Pageof 14