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- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Ectodysplasin research—Where to next?
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