Double Jeopardy: Identification of a Fragile X full mutation associated with Turner Syndrome in a prenatal case

Sara Seneca, A.m. Bael, K; Van Berkel, C. Staessen, Katrien Stouffs, Willy Lissens, Maryse Bonduelle

Research output: Unpublished contribution to conferencePoster

Original languageEnglish
Publication statusPublished - 15 Mar 2013
Event13th Annual meeting of the Belgian Society of Human Genetics - EXPO, Brussels, Belgium
Duration: 15 Mar 201315 Mar 2013

Conference

Conference13th Annual meeting of the Belgian Society of Human Genetics
CountryBelgium
CityBrussels
Period15/03/1315/03/13

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