Paul Bossuyt

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Lut Van Laer, E. H. Huizing, Margriet Verstreken et al. · Nature Genetics · 1998 · 391 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Identification of a Third EXT-like Gene (EXTL3) Belonging to the EXT Gene Family

Wim Van Hul, Wim Wuyts, Jan Hendrickx et al. · Genomics · 1998 · 128 citations

Life Sciences, Genetics, Molecular Genetics +4

Identification and characterization of a novel member of the EXT gene family, EXTL2.

Wim Wuyts, Wim Van Hul, Jan Hendrickx et al. · PubMed · 1998 · 92 citations

Life Sciences, Genetics, Molecular Genetics +3

Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3)

Elke Holinski‐Feder, Edwin Reyniers, Sabine Uhrig et al. · The American Journal of Human Genetics · 2000 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Identification and Characterization of a Novel Member of the EXT Gene Family, EXTL2

Wim Wuyts, Wim Van Hul, Jan Hendrickx et al. · European Journal of Human Genetics · 1997 · 82 citations

Life Sciences, Genetics, Molecular Genetics +3