(Q37026123)

17 August 2017

Genetic analysis of C4 deficiency (English)

1 reference

17 August 2017

Z L Awdeh

1

1 reference

17 August 2017

H D Ochs

series ordinal

2

1 reference

17 August 2017

C A Alper

series ordinal

3

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 January 1981

1 reference

Journal of Clinical Investigation

17 August 2017

1 reference

17 August 2017

67

1 reference

17 August 2017

1

1 reference

17 August 2017

260-263

1 reference

Inherited structural polymorphism of the fourth component of human complement

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Inherited deficiency of the third component of human complement (C′3)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Immunochemical quantitation of antigens by single radial immunodiffusion

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Genetic polymorphism in human glycine-rich beta-glycoprotein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Genetic control of the eighth component of complement

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

International system for human gene nomenclature (1979) ISGN (1979).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Linkage between the Gene (or Genes) Controlling Synthesis of the Fourth Component of Complement and the Major Histocompatibility Complex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Inherited deficiency of the sixth component of complement: a silent or null gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=371595

Genetic polymorphism of human complement C4 and detection of heterozygotes

27 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7451653

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Evidence for a silent or null gene in hereditary C2 deficiency

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7451653

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI110021

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

7451653

1 reference