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The New England Journal of Medicine
|
September 14, 2012
Phenotypic heterogeneity of genomic disorders and rare copy-number variants
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, et al.
Human Mutation
|
September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.
Nature Genetics
|
February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
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Search research articles
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Showing results (81-90 of 83) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 83 results.
The New England Journal of Medicine
|
September 14, 2012
Phenotypic heterogeneity of genomic disorders and rare copy-number variants
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, et al.
Human Mutation
|
September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.
Nature Genetics
|
February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
Page
of 9