Dominique Smeets

Molecular Genetics of X‐Linked Hearing Impairment

C. Cremers, M. Nelen, H. Brunner, 1991, Annals of the New York Academy of Sciences.

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.

H. Smeets, M. Nelen, B. V. van Oost, 1992, The New England journal of medicine.

Familial syndromic esophageal atresia maps to 2p23-p24.

J. Celli, H. Bokhoven, R. Hennekam, 2000, American journal of human genetics.