E. Lachmann

Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity.

J. Sass, I. Knerr, A. Rauch, 2006, Molecular genetics and metabolism.

Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat

T. Papadopoulos, H. Dörr, A. Rauch, 1999, European Journal of Pediatrics.

Deletion of 9q22: a new observation suggesting a specific phenotype.

M. Volleth, W. Schreyer, R. Pfeiffer, 1993, Annales de genetique.