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American Journal of Human Genetics
|
April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Journal of Medical Genetics
|
September 29, 2017
Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature
Manuel Schiff, Céline Roda, Marie-Lorraine Monin, et al.
European Journal of Human Genetics : EJHG
|
April 17, 2014
New insights into genotype-phenotype correlation for GLI3 mutations
Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, et al.
Human Mutation
|
November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis
Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Nature Genetics
|
December 28, 2010
The genome of Theobroma cacao
Xavier Argout, Jerome Salse, Jean-Marc Aury, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Brain : a Journal of Neurology
|
December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
Christopher C Y Mak, Dan Doherty, Angela E Lin, et al.
The American Journal of Gastroenterology
|
August 16, 2017
Dramatic Increase in Incidence of Ulcerative Colitis and Crohn's Disease (1988-2011): A Population-Based Study of French Adolescents
Silvia Ghione, Hélène Sarter, Mathurin Fumery, et al.
Page
of 23
Search research articles
Search
Showing results (221-230 of 228) with videos related to
Sort By:
Page
of 23
You have reached the last page of results.
This site can display upto 228 results.
American Journal of Human Genetics
|
April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.
Journal of Medical Genetics
|
September 29, 2017
Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature
Manuel Schiff, Céline Roda, Marie-Lorraine Monin, et al.
European Journal of Human Genetics : EJHG
|
April 17, 2014
New insights into genotype-phenotype correlation for GLI3 mutations
Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, et al.
Human Mutation
|
November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis
Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Nature Genetics
|
December 28, 2010
The genome of Theobroma cacao
Xavier Argout, Jerome Salse, Jean-Marc Aury, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Brain : a Journal of Neurology
|
December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
Christopher C Y Mak, Dan Doherty, Angela E Lin, et al.
The American Journal of Gastroenterology
|
August 16, 2017
Dramatic Increase in Incidence of Ulcerative Colitis and Crohn's Disease (1988-2011): A Population-Based Study of French Adolescents
Silvia Ghione, Hélène Sarter, Mathurin Fumery, et al.
Page
of 23