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European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 24, 2019
Antenatal diagnosis of cardio-facio-cutaneous syndrome: Prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. About a case and review of literatureJean-Marc Biard, Patricia Steenhaut, Pierre Bernard, et al.British Medical Bulletin|February 12, 2020
Challenges in molecular diagnosis of X-linked Intellectual disabilityChiara De Luca, Valérie Race, Liesbeth Keldermans, et al.Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.Journal of Community Genetics|July 6, 2018
Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR CongoAimé Lumaka, Toni Kasole Lubala, Valérie Race, et al.European Journal of Human Genetics : EJHG|October 10, 2013
Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathyHui Zhao, Valérie Race, Gert Matthijs, et al.Glycobiology|January 23, 2015
Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDGRiet Bammens, Nickita Mehta, Valérie Race, et al.Neurobiology of Aging|July 23, 2013
Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort studySarah Debray, Valérie Race, Veerle Crabbé, et al.European Journal of Neurology|September 1, 2021
RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvementSien H Van Daele, Matthieu Moisse, Valérie Race, et al.Journal of Clinical Laboratory Analysis|March 24, 2017
Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemiaTite Minga Mikobi, Prosper Tshilobo Lukusa, Michel Ntetani Aloni, et al.Orphanet Journal of Rare Diseases|December 12, 2012
COG5-CDG: expanding the clinical spectrumDaisy Rymen, Liesbeth Keldermans, Valérie Race, et al.Pageof 2