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Identification of incompletely penetrant variants and interallelic interactions in autosomal recessive disorders by a population‐genetic approach
Mikó, Ágnes [Mikó, Ágnes (Gyermekgyógyászat), author] I. Department of Pediatrics (SU / FM / C); MTA-SE Lendület Nephrogenetikai Kutatócsoport (SU / FM / C / DP)
;
Kaposi, Ambrus [Kaposi, Ambrus (Típuselmélet), author] Department of Programming Languages And Compilers (ELTE / ELU FoI / ICS); MTA-SE Lendület Nephrogenetikai Kutatócsoport (SU / FM / C / DP)
;
Schnabel, Karolina [Schnabel, Karolina Kornélia (belgyógyászat), author] I. Department of Pediatrics (SU / FM / C); MTA-SE Lendület Nephrogenetikai Kutatócsoport (SU / FM / C / DP)
;
Seidl, Dániel [Seidl, Dániel (gyermekgyógyászat), author] I. Department of Pediatrics (SU / FM / C); MTA-SE Lendület Nephrogenetikai Kutatócsoport (SU / FM / C / DP)
;
Tory, Kálmán ✉ [Tory, Kálmán (gyermekgyógyászat...), author] I. Department of Pediatrics (SU / FM / C); MTA-SE Lendület Nephrogenetikai Kutatócsoport (SU / FM / C / DP)
English Article (Journal Article) Scientific
Published:
HUMAN MUTATION 1059-7794 1098-1004
42
(11)
pp. 1473-1487
2021
SJR Scopus - Genetics (clinical): Q1
Identifiers
MTMT: 32151975
DOI:
10.1002/humu.24273
WoS:
000690653200001
EDIT:
110528
Scopus:
85113597608
PubMed:
34405919
Fundings:
(NKFIA/OTKA KH125566)
(NKFIA/OTKA K135798)
(EFOP-3.6.3-VEKOP16-2017-00009)
(UNKP-18-2-I-SE-63)
(UNKP-19-3-II-SE-13)
(LP2015-1/2015)
Cited in (3)
Citing (7)
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2025-04-26 08:53
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