(Q35830048)

10 August 2017

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies (English)

1 reference

10 August 2017

Lewkonia RM

1

1 reference

10 August 2017

Lin CC

series ordinal

2

1 reference

10 August 2017

Haslam RH

series ordinal

3

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 December 1980

1 reference

Journal of Medical Genetics

10 August 2017

1 reference

10 August 2017

17

1 reference

10 August 2017

6

1 reference

10 August 2017

453-456

1 reference

Absent IgA and deletions of chromosome 18

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Genetic aspects of selective immunoglobulin A deficiency

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Spiramycin the the prevention of postoperative staphylococcal infection

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Immunoglobulin abnormality in a girl with a large chromosome 18.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Genetic studies on human lymphoblastoid cell lines: isozyme and cytogenetic heterogeneity in a cell line, with evidence for localization of the Pep A locus in man

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Sclerosteosis - An autosomal recessive disorder

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885921

Family studies in individuals with selective absence of gamma-A-globulin

24 September 2018

1 reference

12 December 2020

IgA determinants on B-lymphocytes in patients with deficiency of circulating IgA

1 reference

12 December 2020

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus)

1 reference

12 December 2020

IgA deficiency in one of identical twins

1 reference

12 December 2020

Defect in IgA secretion and in IgA specific suppressor cells in patients with selective IgA deficiency

1 reference

12 December 2020

Heavy chain-specific suppression of immunoglobulin synthesis and secretion by lymphocytes from patients with selective IgA deficiency

1 reference

12 December 2020

Identifiers

1 reference

10 August 2017

1 reference