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Jay W Ellison

Showing results (1-10 of 24) with videos related to

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Annual Review of Medicine|October 2, 2012
Genetic basis of intellectual disabilityJay W Ellison, Jill A Rosenfeld, Lisa G Shaffer
American Journal of Medical Genetics. Part A|March 9, 2007
Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problemsYing S Zou, Daniel L Van Dyke, Jay W Ellison
International Journal of Pediatric Otorhinolaryngology|August 18, 2005
Subglottic stenosis in short-statured children: a case for further investigation of airway symptoms in patients with skeletal dysplasiasJonathan H Lee, Jay W Ellison, Gregory J Schears, et al.
Ophthalmic Genetics|April 18, 2009
A novel NDP mutation in an infant with unilateral persistent fetal vasculature and retinal vasculopathyElisabeth P Aponte, Jose S Pulido, Jay W Ellison, et al.
The British Journal of Ophthalmology|November 6, 2012
Retinal mosaicism in a girl with an X-Y translocationCarole G Cherfan, Thomas P Link, Dusica Babovic-Vuksanovic, et al.
Human Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomaliesRegina E Ensenauer, William J Shaughnessy, Syed M Jalal, et al.
The Journal of Surgical Research|August 25, 2007
Evidence of genetic locus heterogeneity for familial bicuspid aortic valveJay W Ellison, Marineh Yagubyan, Ramanath Majumdar, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndromeJustin Overhoff, Marina M Rabideau, Lynne M Bird, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeLisa G Shaffer, Aaron Theisen, Bassem A Bejjani, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Annual Review of Medicine|October 2, 2012
Genetic basis of intellectual disabilityJay W Ellison, Jill A Rosenfeld, Lisa G Shaffer
American Journal of Medical Genetics. Part A|March 9, 2007
Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problemsYing S Zou, Daniel L Van Dyke, Jay W Ellison
International Journal of Pediatric Otorhinolaryngology|August 18, 2005
Subglottic stenosis in short-statured children: a case for further investigation of airway symptoms in patients with skeletal dysplasiasJonathan H Lee, Jay W Ellison, Gregory J Schears, et al.
Ophthalmic Genetics|April 18, 2009
A novel NDP mutation in an infant with unilateral persistent fetal vasculature and retinal vasculopathyElisabeth P Aponte, Jose S Pulido, Jay W Ellison, et al.
The British Journal of Ophthalmology|November 6, 2012
Retinal mosaicism in a girl with an X-Y translocationCarole G Cherfan, Thomas P Link, Dusica Babovic-Vuksanovic, et al.
Human Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomaliesRegina E Ensenauer, William J Shaughnessy, Syed M Jalal, et al.
The Journal of Surgical Research|August 25, 2007
Evidence of genetic locus heterogeneity for familial bicuspid aortic valveJay W Ellison, Marineh Yagubyan, Ramanath Majumdar, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndromeJustin Overhoff, Marina M Rabideau, Lynne M Bird, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeLisa G Shaffer, Aaron Theisen, Bassem A Bejjani, et al.
Pageof 3