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PubMed (OMIM) for id: 854747
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Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia.
Nat Genet. 1999 Aug;22(4):366-9. doi: 10.1038/11937.
Nat Genet. 1999.
PMID: 10431241
A gene for autosomal dominant hypohidrotic ectodermal dysplasia (EDA3) maps to chromosome 2q11-q13.
Ho L, Williams MS, Spritz RA.
Ho L, et al.
Am J Hum Genet. 1998 May;62(5):1102-6. doi: 10.1086/301839.
Am J Hum Genet. 1998.
PMID: 9545409
Free PMC article.
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Autosomal dominant hypohidrotic ectodermal dysplasia in a large family.
Aswegan AL, Josephson KD, Mowbray R, Pauli RM, Spritz RA, Williams MS.
Aswegan AL, et al.
Am J Med Genet. 1997 Nov 12;72(4):462-7. doi: 10.1002/(sici)1096-8628(19971112)72:4<462::aid-ajmg17>3.0.co;2-p.
Am J Med Genet. 1997.
PMID: 9375732
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Autosomal dominant ectodermal dysplasia.
Jorgenson RJ, Dowben JS, Dowben SL.
Jorgenson RJ, et al.
J Craniofac Genet Dev Biol. 1987;7(4):403-12.
J Craniofac Genet Dev Biol. 1987.
PMID: 3429615
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