Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Archives Francaises De Pediatrie|March 1, 1981
[Determination of proteinuria in children: changes in results according to the methods used (author's transl)]R Zawislak, G Vincendon, J Flori, et al.Prenatal Diagnosis|July 1, 1985
Direct fetal chromosome studies from chorionic villiE Flori, I Nisand, J Flori, et al.Journal De Genetique Humaine|February 1, 1981
[Linkage between the gene responsible for adrenal hyperplasia caused by 21-hydroxylase deficiency and chromosome-6 short-arm markers]J Flori, M M Tongio, F Kurtz, et al.Pediatrie|January 1, 1987
[Medical treatment of neonatal chylous ascites: apropos of a case]A Farge, J Pochard, I Nisand, et al.Fetal Diagnosis and Therapy|June 12, 1999
In utero fetal muscle biopsy: a precious aid for the prenatal diagnosis of Duchenne muscular dystrophyS Heckel, R Favre, J Flori, et al.Human Reproduction (Oxford, England)|March 5, 2004
Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case reportE Flori, B Doray, E Gautier, et al.Journal De Genetique Humaine|June 1, 1985
[Determination of fetal karyotype in the first trimester of pregnancy by direct examination of chorionic villi]E Flori, I Nisand, J Flori, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Prenatal diagnosis of a true fetal tetraploidy in direct and cultured chorionic villiC Schluth, B Doray, F Girard-Lemaire, et al.Journal De Genetique Humaine|September 1, 1985
[Correlations between pregnancy pathology, study of the placenta, antenatal echography and examination of the product of conception in a series of 175 congenital malformations]C Stoll, P Curie, B Dott, et al.Journal of Medical Genetics|November 3, 2009
The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screeningC Thauvin-Robinet, A Munck, F Huet, et al.Pageof 1