W. Müller

Familial occurrence of syngnathia congenita syndrome

J. Kofler, I. Gassner, H. Rößler, 1979, Clinical genetics.

Does hyperdiploidy constitute a particular entity in human meningeoma? Cytogenetic studies on 8 cases out of 175 unpublished human meningiomas.

B. Wullich, K. Zang, W. Henn, 1991 .

Congenital factor V deficiency. A family study.

W. Geir, W. Müller, G. Mitterstieler, 2009, Scandinavian journal of haematology.