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Presse Medicale (Paris, France : 1983)|October 19, 2005
[Molecular chromosomic genetics in prenatal and perinatal diagnosis of chromosomal anomalies and genetic diseases]J Lespinasse, G NadeauJournal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Ultrasound abnormalities of the placenta during triploidy with pre-eclampsia in the 2nd trimester]J Salvat, J Lespinasse, A Vincent-Genod, et al.Journal of Intellectual Disability Research : JIDR|March 30, 2007
Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicismA Paoloni-Giacobino, N Lemieux, E Lemyre, et al.Clinical Genetics|September 4, 1998
Phenotypic and genotypic variability in monozygotic triplets with Turner syndromeJ Lespinasse, C Gicquel, M Robert, et al.Annales De Genetique|November 6, 2001
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISHA Paoloni-Giacobino, J Lespinasse, I Moix, et al.Annales De Genetique|January 1, 1996
Identification of a cat eye syndrome using DNA sequence dosage analysisF Bulle, J Lespinasse, A Pawlak, et al.Human Reproduction (Oxford, England)|September 26, 2003
A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failureJ Lespinasse, M O North, C Paravy, et al.Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Six cases of cryptic subtelomeric translocations in four families: the use of subtelomeric FISH probes as a diagnostic toolA Paoloni-Giacobino, S Dahoun, S Briault, et al.Human Reproduction (Oxford, England)|December 4, 2004
Chromosomal instability in two siblings with gonad deficiency: case reportJ Lespinasse, P Hoffmann, A Lauge, et al.Cytogenetics and Cell Genetics|January 1, 1995
Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridizationS Rousseaux, E Chevret, M Monteil, et al.Pageof 3