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International Journal of Andrology|April 9, 1999
Co-localization of HP1 and TP1 transcripts in human spermatids by double electron microscopy in situ hybridizationJ P Siffroi, M F Alfonsi, J P DadouneAnnales De Genetique|January 1, 1986
A cytogenetic analysis of twenty cases of systemic sclerodermaF Romani, F Viguie, J P Siffroi, et al.Gynecologie, Obstetrique & Fertilite|December 29, 2000
[Fetal cells in the maternal blood and prenatal diagnosis]J P Siffroi, N Freiss-Rouas, S Kanafani, et al.Molecular Human Reproduction|July 25, 2000
Y chromosome microdeletions and germinal mosaicism in infertile malesC Le Bourhis, J P Siffroi, K McElreavey, et al.Molecular Human Reproduction|December 14, 2004
Identification of transcripts by macroarrays, RT-PCR and in situ hybridization in human ejaculate spermatozoaJ P Dadoune, A Pawlak, M F Alfonsi, et al.The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|May 23, 2000
Connexin43 gene expression and regulation in the rodent seminiferous epitheliumC Batias, J P Siffroi, P Fénichel, et al.Morphologie : Bulletin De L'Association Des Anatomistes|November 19, 2011
[The Sertoli cell]C Ravel, S JaillardClinical Genetics|November 27, 1998
Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH)B Benzacken, J M Lapierre, J P Siffroi, et al.Molecular Human Reproduction|March 24, 2000
Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidismC Krausz, L Quintana-Murci, M Fellous, et al.Fetal Diagnosis and Therapy|November 14, 1998
Unexpected inherited chromosomal translocation during prenatal diagnosis for maternal age: risk for a nondetectable karyotype imbalance in offspringJ P Siffroi, N Heim, B Benzacken, et al.Pageof 10