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Pigment Cell & Melanoma Research|June 4, 2026
Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation SequencingAnton Karelin, Ines B Brecht, Michaela Pogoda, et al.
Molecular Carcinogenesis|November 19, 2016
Genome-wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastomaJessica Charlet, Ayumi Tomari, Anthony R Dallosso, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 19, 2012
Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE)Deidre R Krupp, Pu-Ting Xu, Sophie Thomas, et al.
American Journal of Human Genetics|May 16, 2007
Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6Christelle Golzio, Jelena Martinovic-Bouriel, Sophie Thomas, et al.
Nature Genetics|March 14, 2007
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisLekbir Baala, Sylvain Briault, Heather C Etchevers, et al.
Pigment Cell & Melanoma Research|March 10, 2026
A Short Report on Melanocyte/Melanoma Culture, Senescence, and ReproducibilityLionel Larue, , Duarte C Barral, et al.
International Journal of Molecular Sciences|July 24, 2021
Somatotroph Tumors and the Epigenetic Status of the <i>GNAS</i> LocusPauline Romanet, Justine Galluso, Peter Kamenicky, et al.
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