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Weimin Bi

Showing results (31-40 of 138) with videos related to

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Human Genetics|March 21, 2018
De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalitiesMagalie S Leduc, Marianne Mcguire, Suneeta Madan-Khetarpal, et al.
Molecular and Cellular Biology|May 2, 2003
Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalanceKatherina Walz, Sandra Caratini-Rivera, Weimin Bi, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Santhosh Girirajan, et al.
Cancer Genetics|August 23, 2024
Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnosesRunjun D Kumar, Liesbeth Vossaert, Weimin Bi, et al.
Plos Genetics|June 2, 2012
A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and menMelanie Lacaria, Pradip Saha, Lorraine Potocki, et al.
American Journal of Medical Genetics. Part A|February 21, 2022
LMOD2-related dilated cardiomyopathy presenting in late infancyErica Lay, Mahshid S Azamian, Susan W Denfield, et al.
American Journal of Medical Genetics. Part A|February 12, 2021
Clinical characterization of individuals with the distal 1q21.1 microdeletionStacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, et al.
American Journal of Obstetrics and Gynecology|October 17, 2017
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratoryAndrea K Petersen, Sau Wai Cheung, Janice L Smith, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadiasSimone Gana, Pierangelo Veggiotti, Giusy Sciacca, et al.
Prenatal Diagnosis|September 17, 2008
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWeimin Bi, Amy M Breman, Susan F Venable, et al.
Pageof 14

Showing results (31-40 of 138) with videos related to

Sort By:
Pageof 14
Human Genetics|March 21, 2018
De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalitiesMagalie S Leduc, Marianne Mcguire, Suneeta Madan-Khetarpal, et al.
Molecular and Cellular Biology|May 2, 2003
Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalanceKatherina Walz, Sandra Caratini-Rivera, Weimin Bi, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndromeWeimin Bi, G Mustafa Saifi, Santhosh Girirajan, et al.
Cancer Genetics|August 23, 2024
Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnosesRunjun D Kumar, Liesbeth Vossaert, Weimin Bi, et al.
Plos Genetics|June 2, 2012
A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and menMelanie Lacaria, Pradip Saha, Lorraine Potocki, et al.
American Journal of Medical Genetics. Part A|February 21, 2022
LMOD2-related dilated cardiomyopathy presenting in late infancyErica Lay, Mahshid S Azamian, Susan W Denfield, et al.
American Journal of Medical Genetics. Part A|February 12, 2021
Clinical characterization of individuals with the distal 1q21.1 microdeletionStacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, et al.
American Journal of Obstetrics and Gynecology|October 17, 2017
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratoryAndrea K Petersen, Sau Wai Cheung, Janice L Smith, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadiasSimone Gana, Pierangelo Veggiotti, Giusy Sciacca, et al.
Prenatal Diagnosis|September 17, 2008
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWeimin Bi, Amy M Breman, Susan F Venable, et al.
Pageof 14