Wieacker, Peter

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Rauch, A., Wieczorek, D., Graf, E., Wieland, T., Endele, S., Schwarzmayr, T., Albrecht, B., Bartholdi, D., Beygo, J., Di Donato, N., et al. (2012) · The Lancet

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

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WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

Bohring, A., Stamm, T., Spaich, C., Haase, C., Spree, K., Hehr, U., Hoffmann, M., Ledig, S., Sel, S., Wieacker, P., et al. (2009) · The American Journal of Human Genetics

dental development and anomaliesGenetic and rare skin diseases.

Cited by 232

Clinical and genetic aspects of craniofrontonasal syndrome: Towards resolving a genetic paradox

Wieacker, P., & Wieland, I. (2005) · Molecular Genetics and Metabolism

Craniofacial Disorders and TreatmentsFetal and Pediatric Neurological Disorders

Cited by 69