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Prenatal Diagnosis|May 29, 1998
High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocationA Guichet, S Briault, C MoraineAnnales De Genetique|January 1, 1996
Trisomy X: ACLF (Association des Cytogénéticiens de Langue Française) retrospective studyA Guichet, S Briault, C Moraine, et al.Clinical Dysmorphology|November 14, 1997
Are t(X;Y) (p22;q11) translocations in females frequently associated with Madelung deformity?A Guichet, S Briault, M Le Merrer, et al.Clinical and Experimental Immunology|November 1, 1988
Isotypy of serum monoclonal immunoglobulins in human immunodeficiency virus-infected adultsS Briault, M Courtois-Capella, F Duarte, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|August 10, 2010
[Fetal hepatosplenomegaly in the third trimester: A sign of leukemia in fetuses with Down syndrome]C Fouché, A Ramos, O Esperandieu, et al.Experimental Eye Research|May 31, 2025
Characterization of gene recombination pattern induced by Tg(Crx-cre)1Tfur mouse strain in visual system organsC Felgerolle, E Villalonga, A Attallah, et al.American Journal of Medical Genetics|August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndromeS Briault, S Odent, J Lucas, et al.Prenatal Diagnosis|October 16, 2002
Prenatal diagnosis of trisomy 21 by i(21q): a rare case of fetoplacental chromosomal discrepancyJ L Gilardi, F Perrotin, C Paillet, 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.Cancer Genetics and Cytogenetics|March 1, 1990
Translocation (8;9)(q12;p21). A new non-random rearrangement in lymphoid malignanciesJ L Huret, A Brizard, P Babin, et al.Pageof 4