About: Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients

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About: Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1983

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) artículu científicu espublizáu en 1983 (ast) наукова стаття, опублікована в січні 1983 (uk) im Januar 1983 veröffentlichter wissenschaftlicher Artikel (de) 1983 թվականի հունվարի 1-ին հրատարակված գիտական հոդված (hy) artikull shkencor i botuar më 01 janar 1983 (sq) scientific article published on 01 January 1983 (en)
publication date	wds:Q72544078-3A9C371F-5311-4A12-997F-5CAC50C27A24
publication date	1983-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72544078-EE06D94B-CE3B-4DEE-83F1-93533B4A051B
language of work or name	English
cites work	wds:Q72544078-1494F975-B96C-4778-AC30-DFBDDF464E80 wds:Q72544078-3672BC96-1EE0-4A71-8B1B-29F77FCD6271 wds:Q72544078-506A38B6-6E08-4C97-B6BC-6A9540BDCB6C wds:Q72544078-5A1C011E-C299-4A3B-A488-4CB082CEBDC7 wds:Q72544078-72D7EC54-F373-425B-B6A8-8603A4F45ABA wds:Q72544078-90A55C87-F2E5-4096-A8B5-95537C6620DA wds:Q72544078-A8175D91-5298-4C05-9848-EDE2492369CF wds:Q72544078-AEA319DD-75FB-400E-8A9A-FCEA37321642 wds:Q72544078-B395AD09-E8F3-4671-8A5C-513957CB987E wds:Q72544078-B3B57EDD-E922-4398-8EC8-6E99A2AC1DF4 wds:Q72544078-C62E3019-CA09-4CDA-8599-73D06F588709 wds:Q72544078-C6AA01B5-404D-434F-BDEC-6EDDB3FB8C6A wds:Q72544078-CD3C7C5D-29B4-4F1F-8E14-264095936499 wds:Q72544078-DB4F555B-4984-4B17-8809-456423AF9C36 wds:Q72544078-DB6BAB4A-27D0-4180-A11E-D3627EC4516D wds:Q72544078-E6B904F0-83ED-49DE-A0C2-2EEFDC7C9130 wds:Q72544078-EC3FE55A-087D-4DB5-9ECA-68F04435A2F2 wds:Q72544078-F55699FE-9D74-42E5-AAF1-A96595BAAD89 wds:Q72544078-FEDEE8BA-AECA-4204-A608-7E6FE91D9035
cites work	Chido and Rodgers blood groups are distinct antigenic components of human complement C4. Genetic polymorphism of human complement C4 and detection of heterozygotes Two HLA-linked loci controlling the fourth component of human complement The location of C2, C4, and BF relative to HLA-B and HLA-D Genetic polymorphism in human glycine-rich beta-glycoprotein Linkage of HL-A and GBG Inherited structural polymorphism of the fourth component of human complement Gene mapping within the T/t complex of the mouse. I. t-Lethal genes are nonallelic Gene mapping within the T/t complex of the mouse. II. Anomalous position of the H-2 complex in t haplotypes Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf International system for human gene nomenclature (1979) ISGN (1979). Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group An Attenuated Form of Congenital Virilizing Adrenal Hyperplasia* Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus A New Antibody Specificity, Anti-Rga, Reacting with a Red Cell and Serum Antigen Linkage and association between HLA and 21-hydroxylase deficiency HLA-A, B, C, DR alleles in congenital adrenal hyperplasia Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complex
author name string	wds:Q72544078-02B8B690-C10F-4855-A512-4BAE636F63E3 wds:Q72544078-2D4E147E-CC1B-4CD0-8C47-6CCC92795CF8 wds:Q72544078-4BB0A8F6-FF8C-49CD-B95E-6EA36F25A7CF wds:Q72544078-72B84302-49C9-4C0F-9888-4D8C8FD2CBDC wds:Q72544078-86596FB4-1A5E-48DB-8882-29B25D0F949A wds:Q72544078-86AD82B7-2A3D-4884-8E35-DD008CAC170D wds:Q72544078-95BF4DB6-681E-43DD-85B7-05A1E45D88B9 wds:Q72544078-D4720756-DBE9-45A5-B48F-B9C7313AF739 wds:Q72544078-FBEBB9D0-90B9-48DB-82D2-7196EC5C626B
author name string	J Granados E J Yunis C A Alper Z L Awdeh C M Giles P S Gerald D Raum E Fleischnick S M Alosco
rdfs:label	Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (en) Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (nl)
skos:prefLabel	Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (en) Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (nl)
name	Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (en) Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (nl)
author	wds:Q72544078-16F0BBC0-B49C-4EEC-99A1-8EAD1C469B7B
author	John Fielding Crigler
title	wds:Q72544078-C3451968-085E-4433-803A-54BD06E01C82
title	Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (en)
page(s)	wds:Q72544078-6F8747D6-B6EB-41CB-B6F3-2D96C3447A5B
page(s)	152-156
instance of	wds:Q72544078-19AFF6B6-809F-423F-99AD-CD0ADE8D63F0
instance of	scholarly article
main subject	wds:Q72544078-DD0F8AFA-A592-4DEF-9D8C-2F49EEAC01D5
main subject	congenital adrenal hyperplasia
PubMed ID	wds:Q72544078-E4DD4BC5-9FC2-4735-9721-1A2E1A6C62B3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6130199
PubMed ID	6130199
published in	wds:Q72544078-A625B322-B166-439E-9EA6-F7BE12FA9D6F
published in	The Lancet
issue	wds:Q72544078-3EFA6201-457D-4CF4-A284-F50DA75DF1CA
volume	wds:Q72544078-BF084713-752F-4123-A313-2253F84317E4
issue	8317
volume	1
DOI	wds:Q72544078-095809B9-E390-45CB-AF66-40DF21902109
DOI	http://dx.doi.org/10.1016/S0140-6736(83)92757-5
DOI	10.1016/S0140-6736(83)92757-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72544078
is cites work of	Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders

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