Literature DB >> 6959378

HLA-A,B,C and haplotype frequencies in the Finnish population.

M L Lokki, M Julin.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1982        PMID： 6959378     DOI： 10.1111/j.1399-0039.1982.tb00352.x

Source DB:  PubMed          Journal:  Tissue Antigens        ISSN： 0001-2815


× No keyword cloud information.
  3 in total

1.  C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.

Authors:  J Partanen; S Koskimies; E Johansson
Journal:  J Med Genet       Date:  1988-06       Impact factor: 6.318

2.  Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.

Authors:  J Partanen; S Koskimies; I Sipilä; V Lipsanen
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

3.  A 'new' DR4 associated D specificity 'JA' in type 1 (insulin-dependent) diabetes: A9, Bw16, DJA, DR4 haplotype.

Authors:  A Mustonen; J Ilonen; H M Surcel; H K Akerblom
Journal:  Diabetologia       Date:  1984-07       Impact factor: 10.122
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.