Martin Zenker

Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.

S. Mundlos, J. Mulliken, A. Aylsworth, 1999, American journal of human genetics.

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

L. Vissers, B. D. de Vries, E. Eichler, 2008, Journal of Medical Genetics.

Neuro-kardio-fazio-kutane Syndrome

V. Mautner, M. Zenker, K. Kutsche, 2010 .

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.

Bethan E. Hoskins, A. Bakkaloğlu, F. Hildebrandt, 2006, Kidney international.

DOCK6 Mutations Are Responsible for a Distinct Autosomal‐Recessive Variant of Adams–Oliver Syndrome Associated with Brain and Eye Anomalies

M. Skalej, B. Tüysüz, H. Kayserili, 2015, Human mutation.