Laurence Olivier-Faivre

Laurence Olivier-Faivre

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Laurence Olivier-Faivre

Laurence Olivier-Faivre

Publications by authors named "Laurence Olivier-Faivre"

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Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability.

J Pediatr 2017 06 8;185:160-166.e1. Epub 2017 Mar 8.

APHP, GH Pitié Salpêtrière, Department of genetics, unit of medical genetics, reference center for intellectual disabilities of rare causes, Paris, France; GRC Intellectual Disability and Autism, UPMC, Paris, France; Sorbonne Universités, UPMC Univ Paris 06, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France; APHP, Hôpital Armand-Trousseau, Department of genetics, Division of clinical genetics, Paris, France.

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http://dx.doi.org/10.1016/j.jpeds.2017.02.023DOI Listing
June 2017

Juvenile xanthogranuloma and nevus anemicus in the diagnosis of neurofibromatosis type 1.

JAMA Dermatol 2014 Jan;150(1):42-6

Dermatology, Centre Hospitalier Universitaire de Dijon3Research Unit EA 4271 Génétique des Anomalies du Développement, Université de Bourgogne, PRES Bourgogne-Franche Comté, France4Centre de Compétence Maladies Rares Neurofibromatose 1, Dijon, France.

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http://dx.doi.org/10.1001/jamadermatol.2013.6434DOI Listing
January 2014