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Annales De Genetique|February 13, 2001
Cytogenetic analysis from DNA by comparative genomic hybridizationG Tachdjian, A Aboura, J M Lapierre, et al.American Journal of Medical Genetics|February 22, 2002
De novo interstitial direct duplication 1(q23.1q31.1) in a fetus with Pierre Robin sequence and camptodactylyA Aboura, A Coulomb-L'Herminé, F Audibert, et al.Cancer Genetics and Cytogenetics|June 27, 2000
Submicroscopic insertion of RARalpha gene into chromosome 15 in two cases of acute promyelocytic leukemiaF Viguié, A Aboura, S Ramond, et al.Clinical Genetics|October 16, 2012
Beckwith-Wiedemann syndrome and long QT syndrome due to familial-balanced translocation t(11;17)(p15.5;q21.3) involving the KCNQ1 geneS Kaltenbach, Y Capri, S Rossignol, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|December 2, 2005
[Cocaine and trisomy 8 associated with prenatal diagnosis of corpus callosum agenesis]E Gonzales, L Caeymaex, A Aboura, et al.Fetal Diagnosis and Therapy|September 11, 2010
Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villiO Anselem, A Bazin, C Mechler, et al.American Journal of Medical Genetics. Part A|March 3, 2007
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardationP Mabboux, S Brisset, A Aboura, et al.Prenatal Diagnosis|November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15A Coulomb L'Herminé, A Aboura, S Brisset, et al.Leukemia|May 28, 2005
Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?F Viguié, A Aboura, D Bouscary, et al.American Journal of Medical Genetics. Part A|October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlationM-L Maurin, S Brisset, M Le Lorc'h, et al.Pageof 3