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Andrologia|May 11, 2012
Molecular cytogenetic and genetic aspects of globozoospermia: a reviewA Perrin, C Coat, M H Nguyen, et al.
Cancer Genetics and Cytogenetics|July 1, 1987
Cytogenetic and biological characterization of two new human plasma cell linesL W Brox, A Belch, E Pollock, et al.
Collegium Antropologicum|February 24, 2001
Microsatellite haplotypes associations with 5 CFTR mutations in "Grande Brière", an isolate located in southern BrittanyS Bezieau, G Picherot, A David, et al.
Cytogenetic and Genome Research|November 15, 2007
Molecular cytogenetics of IGH rearrangements in non-Hodgkin B-cell lymphomaI Bernicot, N Douet-Guilbert, M-J Le Bris, et al.
Gynecologie, Obstetrique & Fertilite|April 23, 2015
[Congenital bilateral absence of vas deferens: From diagnosis to assisted reproductive techniques - the experience of three centers]D Beauvillard, A Perrin, H Drapier, et al.
Human Genetics|December 1, 1992
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French CanadaP Hechtman, B Boulay, M De Braekeleer, et al.
European Journal of Endocrinology|December 10, 2009
45,X/46,XX mosaicism below 30% of aneuploidy: clinical implications in adult women from a reproductive medicine unitL Homer, M-T Le Martelot, F Morel, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 20, 2012
Does 45,X/46,XX mosaicism with 6-28% of aneuploidy affect the outcomes of IVF or ICSI?L Homer, F Morel, F Gallon, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|November 29, 2011
[Azoospermia: management and results: a series of 90 cases]C Coat, A Perrin, M Talagas, et al.
Clinical Genetics|April 29, 1998
Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada)M De Braekeleer, C Mari, C Verlingue, et al.
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