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Human Molecular Genetics
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June 14, 2014
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy
Jeanne L Theis, Michael T Zimmermann, Brandon T Larsen, et al.
American Journal of Human Genetics
|
October 4, 2003
Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients
Regina E Ensenauer, Adewale Adeyinka, Heather C Flynn, et al.
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Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 12 results.
Human Molecular Genetics
|
June 14, 2014
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy
Jeanne L Theis, Michael T Zimmermann, Brandon T Larsen, et al.
American Journal of Human Genetics
|
October 4, 2003
Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients
Regina E Ensenauer, Adewale Adeyinka, Heather C Flynn, et al.
Page
of 2