Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions

Author:

Rosenfeld Jill A.,Crolla John A.,Tomkins Susan,Bader Patricia,Morrow Bernice,Gorski Jerome,Troxell Robin,Forster-Gibson Cynthia,Cilliers Deirdre,Hislop R. Gordon,Lamb Allen,Torchia Beth,Ballif Blake C.,Shaffer Lisa G.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference44 articles.

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3. Spectrum of epilepsy in terminal 1p36 deletion syndrome;Bahi-Buisson;Epilepsia,2008

4. Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2;Ballif;Clin Genet,2008

5. PKC-zeta mediates insulin effects on glucose transport in cultured preadipocyte-derived human adipocytes;Bandyopadhyay;J Clin Endocrinol Metab,2002

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