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Year | Number of Results |
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1998 | 1 |
2007 | 1 |
2008 | 2 |
2011 | 1 |
2024 | 0 |
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Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene.
Am J Med Genet A. 2007 Jul 1;143A(13):1510-3. doi: 10.1002/ajmg.a.31797.
Am J Med Genet A. 2007.
PMID: 17568423
X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families.
Lexner MO, Bardow A, Juncker I, Jensen LG, Almer L, Kreiborg S, Hertz JM.
Lexner MO, et al.
Clin Genet. 2008 Sep;74(3):252-9. doi: 10.1111/j.1399-0004.2008.01037.x. Epub 2008 May 28.
Clin Genet. 2008.
PMID: 18510547
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Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patients.
Conte C, Gambardella S, Bulli C, Rinaldi F, Di Marino D, Falconi M, Bramanti P, Desideri A, Novelli G.
Conte C, et al.
Genet Test. 2008 Sep;12(3):437-42. doi: 10.1089/gte.2008.0020.
Genet Test. 2008.
PMID: 18666859
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Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.
Zhang J, Han D, Song S, Wang Y, Zhao H, Pan S, Bai B, Feng H.
Zhang J, et al.
Eur J Med Genet. 2011 Jul-Aug;54(4):e377-82. doi: 10.1016/j.ejmg.2011.03.005. Epub 2011 Mar 30.
Eur J Med Genet. 2011.
PMID: 21457804
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Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations.
Monreal AW, Zonana J, Ferguson B.
Monreal AW, et al.
Am J Hum Genet. 1998 Aug;63(2):380-9. doi: 10.1086/301984.
Am J Hum Genet. 1998.
PMID: 9683615
Free PMC article.
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