Showing results (41-50 of 74) with videos related to
Sort By:
Pageof 8
BJOG : an International Journal of Obstetrics and Gynaecology|July 11, 2006
Third-trimester fetal MRI in isolated 10- to 12-mm ventriculomegaly: is it worth it?L J Salomon, J Ouahba, A-L Delezoide, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 4, 2007
Comparison between magnetic resonance imaging and fetopathology in the evaluation of fetal posterior fossa non-cystic abnormalitiesB Tilea, A L Delezoide, S Khung-Savatovski, et al.Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.Mechanisms of Development|October 24, 1998
Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossificationA L Delezoide, C Benoist-Lasselin, L Legeai-Mallet, et al.Human Molecular Genetics|April 1, 1996
Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)F Rousseau, V el Ghouzzi, A L Delezoide, et al.Prenatal Diagnosis|December 1, 1994
Prenatal diagnosis of tuberous sclerosis. Use of magnetic resonance imaging and its implications for prognosisH Werner, V Mirlesse, F Jacquemard, et al.Mechanisms of Development|April 27, 2000
Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic developmentM Rachidi, C Lopes, S Gassanova, et al.Genomics|April 2, 1998
Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human developmentF Fougerousse, M Durand, L Suel, et al.Human Genetics|October 28, 1997
Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defectsE Mornet, F Muller, A Lenvoisé-Furet, et al.Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.Pageof 8