F. Hol

A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum

J. van Reeuwijk, T. Roscioli, H. van Bokhoven, 2010, Clinical genetics.

Corneal decompensation in a boy with Kearns-Sayre syndrome

F. Meire, F. Boonstra, I. Claerhout, 2002, Ophthalmic genetics.

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family

E. Mariman, B. Hamel, I. Hansmann, 1995, Human Genetics.

Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation

J. Drenth, A. Lawrence, F. Hol, 2006, Annals of the rheumatic diseases.

A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum

J. van Reeuwijk, T. Roscioli, H. van Bokhoven, 2010, Clinical genetics.

Heterochromia complicata Fuchs

F. Hol, A. Huber, Herrn Prof. Dr, 1988, Klinische Monatsblatter fur Augenheilkunde.