(Q41638857)

5 October 2017

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome (English)

1 reference

5 October 2017

Desmaze C

1

1 reference

5 October 2017

Deleuze JF

2

1 reference

5 October 2017

Dutrillaux AM

3

1 reference

5 October 2017

Thomas G

4

1 reference

5 October 2017

Hadchouel M

5

1 reference

5 October 2017

Aurias A

6

1 reference

5 October 2017

language of work or name

English

0 references

publication date

1 April 1992

1 reference

Journal of Medical Genetics

5 October 2017

1 reference

5 October 2017

29

1 reference

5 October 2017

4

1 reference

5 October 2017

233-235

1 reference

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

5 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

Contiguous gene syndromes: a component of recognizable syndromes

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

Alagille syndrome and deletion of 20p.

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

Molecular cytogenetics: toward dissection of the contiguous gene syndromes

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

Del(20p) with manifestations of arteriohepatic dysplasia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

Localization and linkage of three polymorphic DNA sequences on human chromosome 20

2 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015919

A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1583641

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1583641

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1583641

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.29.4.233

1 reference

5 October 2017

1 reference

5 October 2017

PubMed publication ID

1583641

1 reference