(Q42147378)

English

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

scientific article published on May 1989

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

congenital disorder

0 references

congenital adrenal hyperplasia

1 reference

based on heuristic

inferred from title

author name string

J Partanen

1

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

S Koskimies

2

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

I Sipilä

3

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

V Lipsanen

4

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

language of work or name

0 references

publication date

1 May 1989

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

44

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

5

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

660-670

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Complete sequence of an HLA-dR beta chain deduced from a cDNA clone and identification of multiple non-allelic DR beta chain genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

The structural basis of the multiple forms of human complement component C4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Genetics of adrenal steroid 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Structure of human steroid 21-hydroxylase genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Molecular and clinical advances in congenital adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Phenotyping of human complement component C4, a class-III HLA antigen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Evidence for frequent gene conversion in the steroid 21-hydroxylase P-450(C21) gene: implications for steroid 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715632

29 May 2018

C4B gene polymorphism detected in a human cosmid clone

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new HLA-B7-associated C21-hydroxylase deficiency gene by restriction enzyme length polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-DR-DQ haplotypes defined by restriction fragment analysis. Correlation to serology

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bgl II restriction fragment length polymorphism of human complement C4A gene coincides with BF*F allele of factor B

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/2565078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

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