Ingrid Handig

Postmortem examination of two fragile X brothers with anFMR1 full mutation

Edwin Reyniers, Jean‐Jacques Martin, Patrick Cras et al. · American Journal of Medical Genetics · 1999 · 69 citations

Life Sciences, Genetics, Molecular Genetics +17

Founder effect in a Belgian-Dutch fragile X population

Sonja Buyle, Edwin Reyniers, Lieve Vits et al. · Human Genetics · 1993 · 43 citations

Life Sciences, Genetics, Human Genetics +5

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Guy Van Camp, Marie Neëlle Van Thienen, Ingrid Handig et al. · Journal of Medical Genetics · 1995 · 42 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Apparent regression of the CGG repeat in FMR1 to an allele of normal size

Lieve Vits, Kristel De Boulle, Edwin Reyniers et al. · Human Genetics · 1994 · 34 citations

Life Sciences, Genetics, Molecular Genetics +5

Inheritance of the S113L mutation within an inbred family with carnitine palmitoyltransferase enzyme deficiency

Ingrid Handig, Erna Dams, Franco Taroni et al. · Human Genetics · 1996 · 31 citations

Life Sciences, Genetics, Molecular Genetics +12