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R Chrast

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Clinical Genetics|August 20, 2015

A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani familyK Nikopoulos, G U Butt, P Farinelli, et al.

Genome Research|December 16, 2000

The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normalsR Chrast, H S Scott, M P Papasavvas, et al.

Nature Genetics|January 4, 2001

Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Clinical Genetics|August 20, 2015

A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani familyK Nikopoulos, G U Butt, P Farinelli, et al.

Genome Research|December 16, 2000

Nature Genetics|January 4, 2001

Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.

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