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British Journal of Obstetrics and Gynaecology|July 1, 1998
A multicentre study comparing cervicography and cytology in the detection of cervical intraepithelial neoplasiaP h De Sutter, M Coibion, M Vosse, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterizationP Callier, L Faivre, N Marle, et al.
British Journal of Cancer|July 1, 1994
Is there a role for cervicography in the detection of premalignant lesions of the cervix uteri?M Coibion, P Autier, P Vandam, et al.
Prenatal Diagnosis|March 28, 2007
Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocationC Thauvin-Robinet, P Callier, N Laurent, et al.
European Journal of Medical Genetics|March 23, 2011
Written information to patients in clinical genetics: what's the impact?C Cassini, C Thauvin-Robinet, S Vinault, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|October 16, 2008
Unexpected substitution of dominant rotavirus G genotypes in French hospitalized children over five consecutive seasonsA de Rougemont, J Kaplon, P Lebon, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 27, 2006
Colorectal cancer (CRC) screening using sigmoidoscopy followed by colonoscopy: a feasibility and efficacy study on a cancer institute based populationH Bleiberg, P Autier, F Huet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 11, 2010
[Genetic testing in asymptomatic minors: a survey among French geneticists]L Joly, C Thauvin-Robinet, F Huet, et al.
American Journal of Medical Genetics. Part A|July 17, 2008
Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndromeP Callier, L Faivre, C Thauvin-Robinet, et al.
European Journal of Medical Genetics|November 26, 2008
Tubulopathy and pancytopaenia with normal pancreatic function: a variant of Pearson syndromeAgnès Atale, Patrizia Bonneau-Amati, Agnès Rötig, et al.
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