Гіпогідротична ектодермальна дисплазія (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Гіпогідротична ектодермальна дисплазія" in Ukrainian language version.

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doi.org

dx.doi.org

J Zonana, Elder M. E., Schneider L. C. et al. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO) // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 2000. — Vol. 67, Iss. 6. — P. 1555–62. — ISSN 0002-9297; 1537-6605 — doi:10.1086/316914
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q24538937 d:Track:Q746413
Overbeek P. A. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia // Nature Genetics / M. Axton, T. Faial — NPG, 1999. — Vol. 22, Iss. 4. — P. 366–369. — ISSN 1061-4036; 1546-1718 — doi:10.1038/11937
d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q47528456 d:Track:Q45712608 d:Track:Q22010459

obolibrary.org

purl.obolibrary.org

Disease Ontology — 2016.
d:Track:Q4117183 d:Track:Q5282129

orpha.net

orpha.net/ (англ.). Архів оригіналу за 5 червня 2022. Процитовано 27 березня 2022.

web.archive.org

orpha.net/ (англ.). Архів оригіналу за 5 червня 2022. Процитовано 27 березня 2022.

wikidata.org

J Zonana, J Gault, Davies K. J. et al. Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 1993. — Vol. 52, Iss. 1. — P. 78–84. — ISSN 0002-9297; 1537-6605
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q746413 d:Track:Q35194286
J Zonana, Elder M. E., Schneider L. C. et al. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO) // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 2000. — Vol. 67, Iss. 6. — P. 1555–62. — ISSN 0002-9297; 1537-6605 — doi:10.1086/316914
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q24538937 d:Track:Q746413
Overbeek P. A. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia // Nature Genetics / M. Axton, T. Faial — NPG, 1999. — Vol. 22, Iss. 4. — P. 366–369. — ISSN 1061-4036; 1546-1718 — doi:10.1038/11937
d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q47528456 d:Track:Q45712608 d:Track:Q22010459
Disease Ontology — 2016.
d:Track:Q4117183 d:Track:Q5282129

wikipedia.org

en.wikipedia.org

J Zonana, J Gault, Davies K. J. et al. Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 1993. — Vol. 52, Iss. 1. — P. 78–84. — ISSN 0002-9297; 1537-6605
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q746413 d:Track:Q35194286
J Zonana, Elder M. E., Schneider L. C. et al. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO) // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 2000. — Vol. 67, Iss. 6. — P. 1555–62. — ISSN 0002-9297; 1537-6605 — doi:10.1086/316914
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q24538937 d:Track:Q746413

worldcat.org

J Zonana, J Gault, Davies K. J. et al. Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 1993. — Vol. 52, Iss. 1. — P. 78–84. — ISSN 0002-9297; 1537-6605
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q746413 d:Track:Q35194286
J Zonana, Elder M. E., Schneider L. C. et al. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO) // Am. J. Hum. Genet. — Cell Press, Elsevier BV, 2000. — Vol. 67, Iss. 6. — P. 1555–62. — ISSN 0002-9297; 1537-6605 — doi:10.1086/316914
d:Track:Q4744249 d:Track:Q5058164 d:Track:Q24538937 d:Track:Q746413
Overbeek P. A. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia // Nature Genetics / M. Axton, T. Faial — NPG, 1999. — Vol. 22, Iss. 4. — P. 366–369. — ISSN 1061-4036; 1546-1718 — doi:10.1038/11937
d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q47528456 d:Track:Q45712608 d:Track:Q22010459