Dorothee Cailley
Bordeaux, France
Last Updated: 09/26/2026
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Found 9 publications
Albinism in a patient with mutations at both the OA1 and OCA3 loci.
Journal: Pigment cell & melanoma research
Published: August 07, 2015
Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents.
Journal: American journal of medical genetics. Part A
Published: February 04, 2014
New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.
Journal: American journal of medical genetics. Part A
Published: December 16, 2013
Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Journal: European journal of human genetics : EJHG
Published: September 24, 2013
High-resolution array-CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene.
Journal: Pigment cell & melanoma research
Published: July 30, 2013
Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes.
Journal: European journal of human genetics : EJHG
Published: February 22, 2013
Prenatal diagnosis using array-CGH: a French experience.
Journal: European journal of medical genetics
Published: October 19, 2012
Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures.
Journal: American journal of medical genetics. Part A
Published: December 21, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026