Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-78787-5_41
Reference12 articles.
1. Huang SX, Liang JL, Sui WG, Lin H, Xue W, Chen JJ, Zhang Y, Gong WW, Dai Y, Ou ML (2015) EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature. Genet Mol Res 14(3):10344–103445
2. Mikkola ML (2009) Molecular aspects of hypohidrotic ectodermal dysplasia. Am J Med Genet Part A 149A:2031–2036
3. Anbouba GM, Carmany EP, Natoli JL (2020) The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: a systematic review. Am J Med Genet A 182(4):831–841
4. Reyes-Reali J, Mendoza-Ramos MI, Garrido-Guerrero E, Méndez-Catalá CF, Méndez-Cruz AR, Pozo-Molina G (2018) Hypohidrotic ectodermal dysplasia: clinical and molecular review. Int J Dermatol 57(8):965–972
5. Trzeciak WH, Koczorowski R (2015) Molecular basis of hypohidrotic ectodermal dysplasia: an update. J Appl Genet 57:51–61
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A novel deletion of exon 4 in the Ectodysplasin A gene associated with X-linked hypohidrotic ectodermal dysplasia;Archives of Oral Biology;2023-06
2. Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia;Advances in Experimental Medicine and Biology;2023
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