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Bassem A Bejjani

Showing results (21-30 of 71) with videos related to

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Prenatal Diagnosis|October 2, 2009
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarrayJustine Coppinger, Sarah Alliman, Allen N Lamb, et al.
Expert Opinion on Medical Diagnostics|March 15, 2013
In the middle of it all: a centered approach to chromosome analysisLisa G Shaffer, Blake C Ballif, Aaron Theisen, et al.
Molecular Vision|December 30, 2008
Human anterior chamber angle development without cell death or macrophage involvementBeeran Meghpara, Xin Li, Hiroshi Nakamura, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
American Journal of Medical Genetics|April 27, 2002
Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patientsYuan-Qing Wu, Bassem A Bejjani, Lap-Chee Tsui, et al.
American Journal of Medical Genetics|February 22, 2002
Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocationAndré Mégarbané, Bassem A Bejjani, Lisa G Shaffer, et al.
Prenatal Diagnosis|July 23, 2008
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimensLisa G Shaffer, Justine Coppinger, Sarah Alliman, et al.
The Journal of Molecular Diagnostics : JMD|June 27, 2007
Design, development, validation, and use of synthetic nucleic acid controls for diagnostic purposes and application to cystic fibrosis testingTodd M Christensen, Mohamed Jama, Victor Ponek, et al.
Investigative Ophthalmology & Visual Science|December 8, 2015
Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus FamilyJustyna A Karolak, Malgorzata Rydzanicz, Barbara Ginter-Matuszewska, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|October 2, 2009
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarrayJustine Coppinger, Sarah Alliman, Allen N Lamb, et al.
Expert Opinion on Medical Diagnostics|March 15, 2013
In the middle of it all: a centered approach to chromosome analysisLisa G Shaffer, Blake C Ballif, Aaron Theisen, et al.
Molecular Vision|December 30, 2008
Human anterior chamber angle development without cell death or macrophage involvementBeeran Meghpara, Xin Li, Hiroshi Nakamura, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
American Journal of Medical Genetics|April 27, 2002
Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patientsYuan-Qing Wu, Bassem A Bejjani, Lap-Chee Tsui, et al.
American Journal of Medical Genetics|February 22, 2002
Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocationAndré Mégarbané, Bassem A Bejjani, Lisa G Shaffer, et al.
Prenatal Diagnosis|July 23, 2008
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimensLisa G Shaffer, Justine Coppinger, Sarah Alliman, et al.
The Journal of Molecular Diagnostics : JMD|June 27, 2007
Design, development, validation, and use of synthetic nucleic acid controls for diagnostic purposes and application to cystic fibrosis testingTodd M Christensen, Mohamed Jama, Victor Ponek, et al.
Investigative Ophthalmology & Visual Science|December 8, 2015
Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus FamilyJustyna A Karolak, Malgorzata Rydzanicz, Barbara Ginter-Matuszewska, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Pageof 8