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Bassem A Bejjani

Showing results (11-20 of 71) with videos related to

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The Journal of Pediatrics|November 3, 2004
Expanding the phenotype of alveolar capillary dysplasia (ACD)Partha Sen, Nivedita Thakur, David W Stockton, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
Experimental Eye Research|October 18, 2002
Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyesBassem A Bejjani, Li Xu, Dawna Armstrong, et al.
BMC Medical Genetics|February 14, 2006
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)Seema R Lalani, Trilochan Sahoo, Merideth E Sanders, et al.
The Journal of Molecular Diagnostics : JMD|September 22, 2009
Effects of ozone exposure during microarray posthybridization washes and scanningSteve Byerly, Kyle Sundin, Rajiv Raja, et al.
Genetic Testing and Molecular Biomarkers|April 12, 2011
Multiallelic synthetic quality control material: lessons learned from the cystic fibrosis external quality assessment schemeSarah Berwouts, Todd M Christensen, Jill Brandon, et al.
Molecular Cytogenetics|July 1, 2010
Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGHNicholas J Neill, Beth S Torchia, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part A|August 9, 2008
Williams syndrome in a preterm infant with phenotype of Alagille syndromePrakesh S Shah, Prashanth Murthy, David Skidmore, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the futureLisa G Shaffer, Bassem A Bejjani, Beth Torchia, et al.
Ophthalmic Genetics|July 17, 2004
Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in EcuadorStacey M Curry, Aline G Daou, Pia Hermanns, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|November 3, 2004
Expanding the phenotype of alveolar capillary dysplasia (ACD)Partha Sen, Nivedita Thakur, David W Stockton, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
Experimental Eye Research|October 18, 2002
Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyesBassem A Bejjani, Li Xu, Dawna Armstrong, et al.
BMC Medical Genetics|February 14, 2006
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)Seema R Lalani, Trilochan Sahoo, Merideth E Sanders, et al.
The Journal of Molecular Diagnostics : JMD|September 22, 2009
Effects of ozone exposure during microarray posthybridization washes and scanningSteve Byerly, Kyle Sundin, Rajiv Raja, et al.
Genetic Testing and Molecular Biomarkers|April 12, 2011
Multiallelic synthetic quality control material: lessons learned from the cystic fibrosis external quality assessment schemeSarah Berwouts, Todd M Christensen, Jill Brandon, et al.
Molecular Cytogenetics|July 1, 2010
Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGHNicholas J Neill, Beth S Torchia, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part A|August 9, 2008
Williams syndrome in a preterm infant with phenotype of Alagille syndromePrakesh S Shah, Prashanth Murthy, David Skidmore, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the futureLisa G Shaffer, Bassem A Bejjani, Beth Torchia, et al.
Ophthalmic Genetics|July 17, 2004
Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in EcuadorStacey M Curry, Aline G Daou, Pia Hermanns, et al.
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