(Q33679121)

28 July 2017

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3. (English)

1 reference

28 July 2017

Wolf-Hirschhorn syndrome

1 reference

Kant SG

1

1 reference

28 July 2017

Van Haeringen A

2

1 reference

28 July 2017

Bakker E

3

1 reference

28 July 2017

Stec I

4

1 reference

28 July 2017

Donnai D

5

1 reference

28 July 2017

Mollevanger P

6

1 reference

28 July 2017

Beverstock GC

7

1 reference

28 July 2017

Lindeman-Kusse MC

8

1 reference

28 July 2017

Van Ommen GJ

9

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 July 1997

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

34

1 reference

28 July 2017

7

1 reference

28 July 2017

569-572

1 reference

Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Pitt-Rogers-Danks syndrome: further delineation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

The 1993-94 Généthon human genetic linkage map

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050997

The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9222965

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A girl with the Pitt-Rogers-Danks syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9222965

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.34.7.569

1 reference

28 July 2017

1 reference

28 July 2017

1 reference