Publications by authors named "P Landrieu"

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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, Jérome Maluenda, Dan Mejlachowicz, Pierre Landrieu

J Med Genet· June 2022

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Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability.
Huy Hoang Nguyen, Van Anh Pham, Giulia Barcia, Valérie Malan, Kiem Lien Thi Nguyen, Pierre Landrieu

Am J Med Genet A· September 2018

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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Mathilde Renaud, Maria-Céu Moreira, Bondo Ben Monga, Diana Rodriguez, Rabab Debs, Pierre Landrieu

JAMA Neurol· April 2018

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Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, Carolina Uggenti, Anthony Oojageer, Pierre G Landrieu

Nat Genet· January 2017

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Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, Carolina Uggenti, Anthony Oojageer, Pierre G Landrieu

Nat Genet· October 2016

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