(Q68814333)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3493216%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

title

Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3493216%20AND%20SRC:MED&resulttype=core&format=json

congenital adrenal hyperplasia due to 21-hydroxylase deficiency

27 September 2019

main subject

0 references

author name string

Z Layrisse

1

1 reference

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27 September 2019

C White

2

1 reference

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27 September 2019

P Gunczler

3

1 reference

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27 September 2019

L Gafaro Valera

4

1 reference

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27 September 2019

S Arias

5

1 reference

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27 September 2019

E J Yunis

6

1 reference

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27 September 2019

C A Alper

7

1 reference

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27 September 2019

Z L Awdeh

8

1 reference

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27 September 2019

publication date

1 January 1987

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27 September 2019

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27 September 2019

volume

25

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27 September 2019

issue

2

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27 September 2019

page(s)

99-103

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https://scigraph.springernature.com/pub.10.1007/bf00364274

27 September 2019

exact match

0 references

cites work

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

12 December 2020

Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase

1 reference

12 December 2020

DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex

1 reference

12 December 2020

MHC "supratype" predicting heterozygous 21-hydroxylase deficiency

1 reference

12 December 2020

Inherited structural polymorphism of the fourth component of human complement

1 reference

12 December 2020

Hormonal Phenotype and HLA-Genotype in Families of Patients with Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

1 reference

12 December 2020

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency

1 reference

12 December 2020

Polymorphism of red cell glyoxalase I (EI: 4.4.1.5); a new genetic marker in man. Investigation of 169 mother-child combinations

1 reference

12 December 2020

Microdroplet testing for HLA-A, -B, -C, and -D antigens. The Phillip Levine Award Lecture

1 reference

12 December 2020

Genetic polymorphism of human complement C4 and detection of heterozygotes

1 reference

12 December 2020

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

1 reference

12 December 2020

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing

1 reference

12 December 2020

Interrelationships between Amerindian tribes of lower Amazonia as manifest by HLA haplotype disequilibria

1 reference

12 December 2020

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

1 reference

12 December 2020

Family studies of the HLA system in acute post-streptococcal glomerulonephritis

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00364274

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3493216%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

1 reference