Ulrike Siebers-Renelt

Ulrike Siebers-Renelt

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Ulrike Siebers-Renelt

Ulrike Siebers-Renelt

Publications by authors named "Ulrike Siebers-Renelt"

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SMARCB1 involvement in the development of leiomyoma in a patient with schwannomatosis.

Am J Surg Pathol 2014 Mar;38(3):421-5

*Department of Genome Analysis, Academic Medical Center ∥Department of Pathology, VU University Medical Center, Amsterdam §Department of Pathology, Nijmegen Center for Molecular Life Sciences (NCMLS), Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands †Institute for Human Genetics, University Hospital Muenster, Muenster ‡Institute for Neuropathology, Evangelisches Krankenhaus, Bielefeld, Germany.

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http://dx.doi.org/10.1097/PAS.0000000000000110DOI Listing
March 2014

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

Hum Mutat 2013 Jun 12;34(6):801-11. Epub 2013 Apr 12.

Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://doi.wiley.com/10.1002/humu.22313
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http://dx.doi.org/10.1002/humu.22313DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663886PMC
June 2013