Virginie Vervoort

<i>AGTR2</i> Mutations in X-Linked Mental Retardation

Virginie Vervoort, Michael A. Beachem, Penny S. Edwards et al. · Science · 2002 · 718 citations

Branchio-oto-renal syndrome: The mutation spectrum in<i>EYA1</i>and its phenotypic consequences

Eugene H. Chang, Maithilee Menezes, Nicole C. Meyer et al. · Human Mutation · 2004 · 221 citations

Urology, Genetic Testing, Mendelian Disorder +12

Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome

Virginie Vervoort, Richard J. Smith, Jane O’Brien et al. · European Journal of Human Genetics · 2002 · 54 citations · Full text

Mendelian Disorder, Genetic Disorder, Bor Syndrome +7

<i>POMGnT1</i> gene alterations in a family with neurological abnormalities

Virginie Vervoort, Kenton R. Holden, Kennedy C. Ukadike et al. · Annals of Neurology · 2004 · 34 citations

Developmental Anomaly, Mendelian Disorder, Neurological Abnormalities +12

Sorting nexin 3 (<i>SNX3</i>) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype

Virginie Vervoort · Journal of Medical Genetics · 2002 · 32 citations · Full text