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Blake C Ballif

Showing results (81-90 of 83) with videos related to

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The New England Journal of Medicine|September 14, 2012
Phenotypic heterogeneity of genomic disorders and rare copy-number variantsSanthosh 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 repeatsPaweł 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 delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
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Showing results (81-90 of 83) with videos related to

Sort By:
Pageof 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 variantsSanthosh 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 repeatsPaweł 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 delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
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