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R Eyre

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American Journal of Human Genetics|April 6, 2010

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.

Human Mutation|June 21, 2008

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfectaDustin Baldridge, Ulrike Schwarze, Roy Morello, et al.

Neurology|June 13, 2014

Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS diseaseRussell C Dale, Fabienne Brilot, Lisa V Duffy, et al.

American Journal of Human Genetics|August 27, 2021

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.

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Search research articles

Showing results (231-240 of 234) with videos related to

Sort By:

Pageof 24

You have reached the last page of results.This site can display upto 234 results.

American Journal of Human Genetics|April 6, 2010

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.

Human Mutation|June 21, 2008

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfectaDustin Baldridge, Ulrike Schwarze, Roy Morello, et al.

Neurology|June 13, 2014

Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS diseaseRussell C Dale, Fabienne Brilot, Lisa V Duffy, et al.

American Journal of Human Genetics|August 27, 2021

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.

Pageof 24