Maximilian Muenke

Figure 2. [Schema of the FGFR3 proteinThe...].

Paul Kruszka, Yonit A. Addissie, Nneamaka B. Agochukwu, 2016 .

The use of racial, ethnic, and ancestral categories in human genetics research.

Laura Lyman Rodriguez, Francis S. Collins, Alan E. Guttmacher, 2005, American journal of human genetics.

A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers

Maximilian Muenke, M. Muenke, Yongsu Jeong, 2006, Development.

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

Alexander F. Schier, Rebecca D. Burdine, Jeffrey A. Towbin, 2000, Nature Genetics.

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

George J. Feldman, Andrea Ballabio, Maximilian Muenke, 1997, Nature Genetics.

Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.

Maximilian Muenke, M. Muenke, J. Ming, 2002, American journal of human genetics.

Mutations in the human SIX3 gene in holoprosencephaly are loss of function.

Benjamin Feldman, Maximilian Muenke, S. Bale, 2008, Human molecular genetics.

Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients

Uwe Heinrich, Maximilian Muenke, B. Ertl-Wagner, 2008, American journal of medical genetics. Part A.

When to suspect a genetic syndrome.

Maximilian Muenke, Benjamin D Solomon, M. Muenke, 2012, American family physician.