David Mowat

No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.

Gabriele Gillessen-Kaesbach, Kerstin Kutsche, Martin Zenker, 2008, Clinical dysmorphology.

Mutation spectrum in the large GTPase dynamin 2, and genotype–phenotype correlation in autosomal dominant centronuclear myopathy

Jocelyn Laporte, Luciano Merlini, Christophe Béroud, 2012, Human mutation.

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis.

Joseph Sack, Ethylin Wang Jabs, Amit V Pandey, 2005, American journal of human genetics.