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Journal of Neurology|August 14, 2001
The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disordersV Pingault, N Bondurand, C Le Caignec, et al.
Prenatal Diagnosis|December 10, 2003
Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2pC Le Caignec, N Winer, M Boceno, et al.
Clinical Genetics|June 6, 2003
Mapping a gene for 46,XY gonadal dysgenesis by linkage analysisD Jawaheer, S-H H Juo, C Le Caignec, et al.
Prenatal Diagnosis|April 2, 2004
Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylationC Le Caignec, C Gicquel, M C Gubler, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 23, 2003
Prenatal diagnosis of a cleidocranial dysplasia-like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocationN Winer, C Le Caignec, M P Quere, et al.
Human Reproduction (Oxford, England)|February 7, 2007
Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case reportG Joly-Helas, C de La Rochebrochard, N Mousset-Siméon, et al.
Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.
Clinical Genetics|August 2, 2011
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1BC Halgren, S Kjaergaard, M Bak, et al.
International Journal of Obesity (2005)|December 2, 2015
16p11.2 Locus modulates response to satiety before the onset of obesityA M Maillard, L Hippolyte, B Rodriguez-Herreros, et al.
Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.
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