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Showing results (61-70 of 66) with videos related to

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Clinical Genetics|March 19, 2010
Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.
Leukemia|October 14, 2006
Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique HématologiqueB Cauwelier, H Cavé, C Gervais, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Clinical Genetics|March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disabilityP Callier, B Aral, N Hanna, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Clinical Genetics|March 19, 2010
Delineation of 15q13.3 microdeletionsA Masurel-Paulet, J Andrieux, P Callier, et al.
Leukemia|October 14, 2006
Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique HématologiqueB Cauwelier, H Cavé, C Gervais, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Clinical Genetics|March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disabilityP Callier, B Aral, N Hanna, et al.
Pageof 7