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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
July 1, 2004
Brown syndrome associated with velocardiofacial syndrome
Susie Chang, Carol A Crowe, Elias I Traboulsi
The American Journal of Cardiology
|
June 1, 2014
Left ventricular dysfunction in duchenne muscular dystrophy and genotype
Mahi L Ashwath, Irwin B Jacobs, Carol A Crowe, et al.
Journal of Child Neurology
|
May 27, 2010
Cardiac and pulmonary function variability in Duchenne/Becker muscular dystrophy: an initial report
David J Birnkrant, Mahi Lakshmi Ashwath, Garey H Noritz, et al.
Human Genetics
|
May 19, 2009
Regional genomic instability predisposes to complex dystrophin gene rearrangements
Junko Oshima, Daniel B Magner, Jennifer A Lee, et al.
American Journal of Medical Genetics. Part A
|
May 15, 2012
Germline mosaicism in Cornelia de Lange syndrome
Thomas P Slavin, Noam Lazebnik, Dinah M Clark, et al.
Human Mutation
|
September 18, 2010
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations
Juergen Scharner, Charlotte A Brown, Matthew Bower, et al.
Human Mutation
|
March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy
Johann Böhm, Valérie Biancalana, Elizabeth T Dechene, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
July 1, 2004
Brown syndrome associated with velocardiofacial syndrome
Susie Chang, Carol A Crowe, Elias I Traboulsi
The American Journal of Cardiology
|
June 1, 2014
Left ventricular dysfunction in duchenne muscular dystrophy and genotype
Mahi L Ashwath, Irwin B Jacobs, Carol A Crowe, et al.
Journal of Child Neurology
|
May 27, 2010
Cardiac and pulmonary function variability in Duchenne/Becker muscular dystrophy: an initial report
David J Birnkrant, Mahi Lakshmi Ashwath, Garey H Noritz, et al.
Human Genetics
|
May 19, 2009
Regional genomic instability predisposes to complex dystrophin gene rearrangements
Junko Oshima, Daniel B Magner, Jennifer A Lee, et al.
American Journal of Medical Genetics. Part A
|
May 15, 2012
Germline mosaicism in Cornelia de Lange syndrome
Thomas P Slavin, Noam Lazebnik, Dinah M Clark, et al.
Human Mutation
|
September 18, 2010
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations
Juergen Scharner, Charlotte A Brown, Matthew Bower, et al.
Human Mutation
|
March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy
Johann Böhm, Valérie Biancalana, Elizabeth T Dechene, et al.
Page
of 1