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Lars R Jensen

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European Journal of Human Genetics : EJHG|January 27, 2011

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1Lars R Jensen, Wei Chen, Bettina Moser, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 2011

Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humansChanghui Pak, Masoud Garshasbi, Kimia Kahrizi, et al.

Nature Genetics|November 25, 2003

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardationVera M Kalscheuer, Kristine Freude, Luciana Musante, et al.

Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018

A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 44 results.

European Journal of Human Genetics : EJHG|January 27, 2011

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1Lars R Jensen, Wei Chen, Bettina Moser, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 2011

Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humansChanghui Pak, Masoud Garshasbi, Kimia Kahrizi, et al.

Nature Genetics|November 25, 2003

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardationVera M Kalscheuer, Kristine Freude, Luciana Musante, et al.

Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018

A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.

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