L. Wehner

SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome

D. Horn, S. Mundlos, J. Allanson, 2007, Journal of Medical Genetics.

Herpesvirus saimiri Tip gene causes T-cell lymphomas in transgenic mice.

U. Rüther, B. Biesinger, U. Friedrich, 2001, DNA and cell biology.

ALK‐1 mutations in liver transplanted patients with hereditary hemorrhagic telangiectasia

P. Neuhaus, W. Engel, K. Nayernia, 2005, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Involvement of fungi other than Rhizoctonia solani in crater disease of wheat

L. Wehner, F. Meyer, 2000 .

Mutation analysis of the M6b gene in patients with Pelizaeus-Merzbacher-like syndrome.

H. Hennies, M. Henneke, J. Gärtner, 2004, American journal of medical genetics. Part A.

Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

Stefan Mundlos, Denise Horn, Dirk Schnabel, 2006, Journal of Medical Genetics.

Germline KRAS mutations cause Noonan syndrome

Kam Y. J. Zhang, Erik Sistermans, Kam Y J Zhang, 2006, Nature Genetics.

[Pulmonary hypertension in hereditary haemorrhagic teleangiectasia].

H. Ghofrani, F. Reichenberger, R. Voswinckel, 2009, Pneumologie.

Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations

W. Engel, K. Nayernia, Werner Ja, 2006, Clinical genetics.

Mutation analysis of the M6b gene in patients with Pelizaeus–Merzbacher‐like syndrome

H. Hennies, M. Henneke, J. Gärtner, 2004 .

Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia.

W. Engel, K. Nayernia, L. Wehner, 2006, International journal of molecular medicine.

Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

E. Roeder, D. Cummings, H. Smeets, 2009, Journal of Medical Genetics.