Publications by authors named "Camille Leroy"

8Publications

Fetal phenotype associated with the 22q11 deletion.

Am J Med Genet A 2014 Nov 8;164A(11):2724-31. Epub 2014 Aug 8.

Service de Génétique et Biologie de la Reproduction, Hôpital Maison Blanche, Centre Hospitalier Universitaire, Reims, France.

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http://dx.doi.org/10.1002/ajmg.a.36720DOI Listing
November 2014

De novo deletion of TBL1XR1 in a child with non-specific developmental delay supports its implication in intellectual disability.

Am J Med Genet A 2014 Sep 28;164A(9):2335-7. Epub 2014 May 28.

Department of Genetics, APHP-Robert DEBRE University Hospital, Paris VII-Denis Diderot Medical School and INSERM UMR 1141 "PROTECT", Paris, France.

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http://dx.doi.org/10.1002/ajmg.a.36619DOI Listing
September 2014

Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion.

Eur J Med Genet 2012 Nov 4;55(11):625-9. Epub 2012 Aug 4.

Department of Child and Adolescent Psychiatry, University Hospital of Reims, France.

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http://dx.doi.org/10.1016/j.ejmg.2012.07.009DOI Listing
November 2012

A familial syndromal form of omphalocele.

Eur J Med Genet 2011 May-Jun;54(3):337-40. Epub 2011 Feb 17.

Clinical Genetics Unit, University Hospital, Pointe-à-Pitre University Hospital, Guadalupe Island, France.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212110001
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http://dx.doi.org/10.1016/j.ejmg.2011.02.001DOI Listing
September 2011