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Journal of the Peripheral Nervous System : JPNS|February 19, 2016
Late onset dHMN II caused by c.404C>G mutation in HSPB1 geneMoritz Oberstadt, Diana Mitter, Joseph Classen, et al.
American Journal of Medical Genetics. Part A|February 8, 2008
Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous fatherDiana Mitter, Deborah Krakow, Claire Farrington-Rock, et al.
The Journal of Endocrinology|May 31, 2007
Estrogen receptor {beta}1 exerts antitumoral effects on SK-OV-3 ovarian cancer cellsOliver Treeck, Georg Pfeiler, Diana Mitter, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspringAndreas Rump, Laura Hildebrand, Andreas Tzschach, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 30, 2016
A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findingsBardo Wannenmacher, Diana Mitter, Franziska Kießling, et al.
Clinical Endocrinology|June 30, 2015
Novel peroxisome proliferator-activated receptor gamma mutation in a family with familial partial lipodystrophy type 3Konstanze Miehle, Joseph Porrmann, Diana Mitter, et al.
Familial Cancer|May 30, 2008
Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastomaDiana Mitter, Diane Rushlow, Inga Nowak, et al.
Journal of Neurochemistry|June 17, 2004
The synaptophysin/synaptobrevin complex dissociates independently of neuroexocytosisClemens Reisinger, Sowmya V Yelamanchili, Britta Hinz, et al.
European Journal of Human Genetics : EJHG|April 21, 2011
Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletionsDiana Mitter, Reinhard Ullmann, Artur Muradyan, et al.
American Journal of Medical Genetics. Part A|July 26, 2017
Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalitiesDenise Horn, Eberhard Siebert, Ulrich Seidel, et al.
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