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Prenatal Diagnosis|August 1, 1995
Prenatal diagnosis of trisomy 8 mosaicism in CVS after abnormal ultrasound findings at 12 weeksA Guichet, S Briault, A Toutain, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three familiesM Raynaud, M P Moizard, B Dessay, et al.American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.Experimental Eye Research|October 20, 2022
FMR protein: Evidence of an emerging role in retinal aging?M Ardourel, I Ranchon-Cole, A Pâris, et al.Annales De Dermatologie Et De Venereologie|October 21, 2006
[Increased haemoglobin A2 levels in pseudoxanthoma elasticum]L Martin, S Pissard, P Blanc, et al.Cancer Genetics and Cytogenetics|June 1, 1992
Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemiaC Barin, C Valtat, S Briault, et al.Clinical Genetics|March 1, 1994
X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric regionC Gendrot, N Ronce, A Toutain, et al.Prenatal Diagnosis|September 5, 2002
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counsellingB Gilbert, C Yardin, S Briault, et al.Annales De Genetique|January 1, 1993
X-linked alpha-thalassemia/mental retardation syndrome. Linkage analysis in a new family further supports localization in proximal XqC I Houdayer, A Toutain, N Ronce, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|February 24, 2005
[Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation]J E Forissier, G Bonne, C Bouchier, et al.Pageof 4