Johnson-McMillin-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Johnson-McMillin-Syndrom" in German language version.

refsWebsite

Global rank German rank

1zdb-katalog.de

123^rd place

6^th place

2^nd place

3^rd place

4^th place

7^th place

3,537^th place

429^th place

doi.org

V. P. Johnson, J. M. McMillin, T. Aceto, G. Bruins: A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism. In: American journal of medical genetics. Bd. 15, Nr. 3, Juli 1983, ISSN 0148-7299, S. 497–506, doi:10.1002/ajmg.1320150316, PMID 6881216.

nih.gov

ncbi.nlm.nih.gov

V. P. Johnson, J. M. McMillin, T. Aceto, G. Bruins: A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism. In: American journal of medical genetics. Bd. 15, Nr. 3, Juli 1983, ISSN 0148-7299, S. 497–506, doi:10.1002/ajmg.1320150316, PMID 6881216.

orpha.net

Eintrag zu Neuroektodermales Syndrom Typ Johnson. In: Orphanet (Datenbank für seltene Krankheiten)

zdb-katalog.de

V. P. Johnson, J. M. McMillin, T. Aceto, G. Bruins: A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism. In: American journal of medical genetics. Bd. 15, Nr. 3, Juli 1983, ISSN 0148-7299, S. 497–506, doi:10.1002/ajmg.1320150316, PMID 6881216.