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Jay W Ellison

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Neurogenetics|January 6, 2012

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.

Human Mutation|July 24, 2013

Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.

American Journal of Medical Genetics. Part A|March 16, 2013

Investigation of NRXN1 deletions: clinical and molecular characterizationMindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, et al.

European Journal of Human Genetics : EJHG|April 9, 2015

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndromeJulián Nevado, Jill A Rosenfeld, Rocío Mena, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 24 results.

Neurogenetics|January 6, 2012

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.

Human Mutation|July 24, 2013

Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.

American Journal of Medical Genetics. Part A|March 16, 2013

Investigation of NRXN1 deletions: clinical and molecular characterizationMindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, et al.

European Journal of Human Genetics : EJHG|April 9, 2015

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndromeJulián Nevado, Jill A Rosenfeld, Rocío Mena, et al.

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