R. D. Lagelouse

Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene.

K. Schwarz, A. Fischer, G. de Saint Basile, 1996, The Journal of pediatrics.

Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.

J. Weissenbach, D. Le Paslier, D. Paslier, 1996, American journal of human genetics.