Search
forResearch 10 of 43
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- 1430 Modeling the onset of senescence associated secretory phenotype predicts therapeutic targets
- NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: A new disease association
- The Genetics of Human Skin Disease
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →