Publications by authors named "M P Geurds"

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Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X).
F A Hol, M P Geurds, C W Cremers, B C Hamel, E C Mariman

Hum Mutat· June 1999

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Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.
A Silahtaroglu, F A Hol, P K Jensen, M Erdel, H C Duba, M P Geurds

Eur J Hum Genet· January 1999

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Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects.
F A Hol, N M van der Put, M P Geurds, S G Heil, F J Trijbels

Clin Genet· February 1998

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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.
F A Hol, M P Geurds, S Chatkupt, Y Y Shugart, R Balling

J Med Genet· August 1996

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Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.
F A Hol, B C Hamel, M P Geurds, I Hansmann, F A Nabben

Hum Genet· June 1995

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