外异蛋白A受体 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "外异蛋白A受体" in Chinese language version.

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doi.org (Global: 2^nd place; Chinese: 23^rd place)

Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics. August 1999, 22 (4): 366–9. PMID 10431241. S2CID 11348633. doi:10.1038/11937.
Aswegan AL, Josephson KD, Mowbray R, Pauli RM, Spritz RA, Williams MS. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. American Journal of Medical Genetics. November 1997, 72 (4): 462–7. PMID 9375732. doi:10.1002/(SICI)1096-8628(19971112)72:4<462::AID-AJMG17>3.0.CO;2-P.

Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics. August 1999, 22 (4): 366–9. PMID 10431241. S2CID 11348633. doi:10.1038/11937.
Aswegan AL, Josephson KD, Mowbray R, Pauli RM, Spritz RA, Williams MS. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. American Journal of Medical Genetics. November 1997, 72 (4): 462–7. PMID 9375732. doi:10.1002/(SICI)1096-8628(19971112)72:4<462::AID-AJMG17>3.0.CO;2-P.
Entrez Gene: EDAR ectodysplasin A receptor. [2023-03-05]. （原始内容存档于2010-03-07）.

Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics. August 1999, 22 (4): 366–9. PMID 10431241. S2CID 11348633. doi:10.1038/11937.