Found: 6
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Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12189, doi. 10.3390/ijms232012189
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- Publication type:
- Article
Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant.
- Published in:
- European Journal of Pediatrics, 2022, v. 181, n. 1, p. 413, doi. 10.1007/s00431-021-04221-w
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- Article
No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
- Published in:
- 2021
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- Publication type:
- journal article
Functional and clinical analysis of five EDA variants associated with ectodermal dysplasia but with a hard-to-predict significance.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.934395
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- Publication type:
- Article
Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia.
- Published in:
- Genes, 2023, v. 14, n. 1, p. 153, doi. 10.3390/genes14010153
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- Publication type:
- Article
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update.
- Published in:
- Genes, 2022, v. 13, n. 12, p. 2327, doi. 10.3390/genes13122327
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- Publication type:
- Article