(Q42662304)

4 November 2017

Renal and urological tract malformations caused by a 22q11 deletion (English)

1 reference

4 November 2017

Devriendt K

1

1 reference

4 November 2017

Swillen A

2

1 reference

4 November 2017

Fryns JP

3

1 reference

4 November 2017

Proesmans W

4

1 reference

4 November 2017

Gewillig M

5

1 reference

4 November 2017

language of work or name

English

0 references

publication date

1 April 1996

1 reference

Journal of Medical Genetics

4 November 2017

1 reference

4 November 2017

33

1 reference

4 November 2017

4

1 reference

4 November 2017

349

1 reference

Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

DiGeorge syndrome: part of CATCH 22.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

Embryologic basis for lower ureteral anomalies: a hypothesis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

The spectrum of the DiGeorge syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

Clinical and molecular study of DiGeorge sequence.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050591

The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patients

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8730297

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hereditary renal adysplasia: new observations and hypotheses

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8730297

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.33.4.349

1 reference

4 November 2017

1 reference

4 November 2017

PubMed publication ID

8730297

1 reference