Genesis of Two Most Prevalent Prop1 Gene Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations

AuthID
 P-00K-5T4
21
Author(s)
Dusatkova, P
·
Pfaeffle, R
·
Brown, MR
·
Akulevich, N
·
Arnhold, IJP
·
Kalina, MA
·
Kot, K
·
[+1]·
Cinek, O
·
Blum, WF
·
Parks, JS
·
Lebl, J
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Document Type
Article
Year published
2016
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 24, Issue: 3, Pages: 415-420 (6)
Indexing
Wos®
Scopus®
Crossref®27
Google Scholar®
Publication Identifiers
SCOPUS: 2-s2.0-84958111231
Wos: WOS:000370469500021
Source Identifiers
ISSN: 1018-4813
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All authors
Name Order Name   Name Order Name   Name Order Name
1 Dusatkova, P;   2 Pfaeffle, R;   3 Brown, MR;
4 Akulevich, N;   5 Arnhold, IJP;   6 Kalina, MA;
7 Kot, K;   8 Krzisnik, C;   9 Lemos, MC;
10 Malikova, J;   11 Navardauskaite, R;   12 Obermannova, B;
13 Pribilincova, Z;   14 Sallai, A;   15 Stipancic, G;
16 Verkauskiene, R;   17 Cinek, O;   18 Blum, WF;
19 Parks, JS;   20 Austerlitz, F;   21 Lebl, J;

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