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- Q84893331 description "artículu científicu espublizáu en payares de 2012" @default.
- Q84893331 description "im November 2012 veröffentlichter wissenschaftlicher Artikel" @default.
- Q84893331 description "scientific article published on 01 November 2012" @default.
- Q84893331 description "wetenschappelijk artikel" @default.
- Q84893331 description "наукова стаття, опублікована в листопаді 2012" @default.
- Q84893331 name "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 name "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 type Item @default.
- Q84893331 label "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 label "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 prefLabel "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 prefLabel "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 P1433 Q84893331-4BE76B02-9D56-4F1C-A904-6A37A26CE93F @default.
- Q84893331 P1476 Q84893331-EBFD4744-116F-467D-BD6C-3336AEF23415 @default.
- Q84893331 P2093 Q84893331-2A8A5268-DD9C-47E8-9535-099DE3BDE5AC @default.
- Q84893331 P2093 Q84893331-38B6D905-6895-4121-AB6C-379345A57ABC @default.
- Q84893331 P2093 Q84893331-64643080-8033-4FB9-8CFD-3AC010FFA25C @default.
- Q84893331 P2093 Q84893331-CCE01656-78F5-4923-B00D-ACEFAAB0612F @default.
- Q84893331 P304 Q84893331-8BBDA888-E7AA-46EA-8053-F2E90CD735B4 @default.
- Q84893331 P31 Q84893331-CAD74FFB-7560-438D-9F20-6A2C18436FE4 @default.
- Q84893331 P356 Q84893331-8AE04513-D8F2-4160-B7D8-06089F26C6AB @default.
- Q84893331 P433 Q84893331-B535727D-C683-459F-9E75-EE881A32080C @default.
- Q84893331 P478 Q84893331-9BFC56B8-EB53-4910-9CEC-F1CA580DFFF0 @default.
- Q84893331 P577 Q84893331-509FE4AE-61BC-4A3B-ACD3-8A678B5D6DBD @default.
- Q84893331 P698 Q84893331-DB481262-5E11-4854-8EF9-21327060B028 @default.
- Q84893331 P921 Q84893331-34783972-BD91-4852-9D5A-7A2CC4274E0B @default.
- Q84893331 P356 J.1651-2227.2012.02823.X @default.
- Q84893331 P698 22931312 @default.
- Q84893331 P1433 Q4676739 @default.
- Q84893331 P1476 "Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II" @default.
- Q84893331 P2093 "Casper L Jessen" @default.
- Q84893331 P2093 "Jane H Christensen" @default.
- Q84893331 P2093 "Niels H Birkebaek" @default.
- Q84893331 P2093 "Soren Rittig" @default.
- Q84893331 P304 "e519-25" @default.
- Q84893331 P31 Q13442814 @default.
- Q84893331 P356 "10.1111/J.1651-2227.2012.02823.X" @default.
- Q84893331 P433 "11" @default.
- Q84893331 P478 "101" @default.
- Q84893331 P577 "2012-11-01T00:00:00Z" @default.
- Q84893331 P698 "22931312" @default.
- Q84893331 P921 Q114049690 @default.