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The Journal of Clinical Endocrinology and Metabolism|March 23, 2016
Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian InsufficiencyC Hyon, L Mansour-Hendili, S Chantot-Bastaraud, et al.Journal of Medical Genetics|December 10, 1997
Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephalyB Benzacken, J P Siffroi, C Le Bourhis, et al.Human Reproduction (Oxford, England)|December 1, 2000
Sex chromosome mosaicism in males carrying Y chromosome long arm deletionsJ P Siffroi, C Le Bourhis, C Krausz, et al.Human Reproduction (Oxford, England)|June 19, 2018
Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinomaN Bourcigaux, C Rubino, I Berthaud, et al.Gynecologie, Obstetrique & Fertilite|May 19, 2009
[Spermiogenesis: histone acetylation triggers male genome reprogramming]S Rousseaux, J Gaucher, J Thevenon, et al.Fetal Diagnosis and Therapy|June 27, 2000
Usefulness of fluorescence in situ hybridization for the diagnosis of Turner mosaic fetuses with small ring X chromosomesJ P Siffroi, O Dupuy, N Joye, et al.The Journal of Clinical Endocrinology and Metabolism|October 16, 1999
A high frequency of Y chromosome deletions in males with nonidiopathic infertilityC Krausz, L Quintana-Murci, S Barbaux, et al.Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.Pageof 5