Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients (Q72544078)

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27 October 2019

title

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

1 reference

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congenital adrenal hyperplasia

27 October 2019

main subject

1 reference

inferred from title

author

John Fielding Crigler

6

object named as

J F Crigler

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27 October 2019

author name string

E Fleischnick

1

1 reference

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27 October 2019

Z L Awdeh

2

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27 October 2019

D Raum

3

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27 October 2019

J Granados

4

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27 October 2019

S M Alosco

5

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27 October 2019

P S Gerald

7

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27 October 2019

C M Giles

8

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27 October 2019

E J Yunis

9

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27 October 2019

C A Alper

10

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27 October 2019

language of work or name

English

0 references

publication date

1 January 1983

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27 October 2019

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27 October 2019

volume

1

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issue

8317

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page(s)

152-156

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An Attenuated Form of Congenital Virilizing Adrenal Hyperplasia*

27 October 2019

cites work

1 reference

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7 January 2021

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

1 reference

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7 January 2021

Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group

1 reference

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7 January 2021

Linkage and association between HLA and 21-hydroxylase deficiency

1 reference

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7 January 2021

Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complex

1 reference

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7 January 2021

HLA-A, B, C, DR alleles in congenital adrenal hyperplasia

1 reference

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7 January 2021

Linkage of HL-A and GBG

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Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf

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Two HLA-linked loci controlling the fourth component of human complement

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7 January 2021

Inherited structural polymorphism of the fourth component of human complement

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Chido and Rodgers blood groups are distinct antigenic components of human complement C4.

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The location of C2, C4, and BF relative to HLA-B and HLA-D

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7 January 2021

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus

1 reference

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7 January 2021

Genetic polymorphism in human glycine-rich beta-glycoprotein

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7 January 2021

Genetic polymorphism of human complement C4 and detection of heterozygotes

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A New Antibody Specificity, Anti-Rga, Reacting with a Red Cell and Serum Antigen

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7 January 2021

Gene mapping within the T/t complex of the mouse. I. t-Lethal genes are nonallelic

1 reference

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7 January 2021

Gene mapping within the T/t complex of the mouse. II. Anomalous position of the H-2 complex in t haplotypes

1 reference

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7 January 2021

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Identifiers

DOI

1 reference

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27 October 2019

1 reference