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Tijdschrift Voor Kindergeneeskunde|June 1, 1993
[Dysmaturity as symptom of the ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome]L Porcelijn, J A Maat-Kievit, A van HaeringenNederlands Tijdschrift Voor Geneeskunde|November 29, 2001
[From gene to disease; HD gene and Huntington disease]J A Maat-Kievit, M Losekoot, R A RoosClinical Dysmorphology|January 1, 1994
Total situs inversus associated with the oculo-auriculo-vertebral spectrumJ A Maat-Kievit, M Baraitser, R M WinterClinical Genetics|January 6, 2007
Diagnosis and management of early- and late-onset cerebellar ataxiaE Brusse, J A Maat-Kievit, J C van SwietenClinical Dysmorphology|April 1, 1994
A case with blepharophimosis resembling Ohdo syndromeJ A Maat-Kievit, P J Milla, J E Collins, et al.Nederlands Tijdschrift Voor Geneeskunde|August 21, 1993
[Phenylketonuria in spite of screening]P D Maaswinkel-Mooij, J E Kist-van Holthe tot Echten, J A Maat-KievitPrenatal Diagnosis|May 1, 1993
A large retinoblastoma detected in a fetus at 21 weeks of gestationJ A Maat-Kievit, D Oepkes, N G Hartwig, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 23, 2000
Family history and DNA analysis in patients with suspected Huntington's diseaseS Siesling, M Vegter-van de Vlis, M Losekoot, et al.Journal of Medical Genetics|April 16, 1999
Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacitiesA T Helderman-van den Enden, P D Maaswinkel-Mooij, E Hoogendoorn, et al.Genomics|October 1, 1990
Genetic heterogeneity in tuberous sclerosisL A Janssen, L A Sandkuyl, E C Merkens, et al.Pageof 2