(Q33676360)

28 July 2017

title

Alagille syndrome: family studies (English)

1 reference

28 July 2017

0 references

1 reference

F. V. Elmslie

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

A. J. Vivian

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

H. Gardiner

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

C. Hall

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

A. P. Mowat

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

R. M. Winter

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

9 July 2024

language of work or name

English

0 references

publication date

1 April 1995

1 reference

full work available at URL

28 July 2017

https://jmg.bmj.com/content/jmedgenet/32/4/264.full.pdf

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

https://europepmc.org/articles/PMC1050372

9 July 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

https://europepmc.org/articles/PMC1050372?pdf=render

9 July 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7643353

https://syndication.highwire.org/content/doi/10.1136/jmg.32.4.264

9 July 2024

1 reference

https://api.crossref.org/works/10.1136/JMG.32.4.264

Journal of Medical Genetics

9 July 2024

published in

1 reference

28 July 2017

volume

32

1 reference

28 July 2017

issue

4

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28 July 2017

page(s)

264-268

1 reference

Segregation analysis of Alagille syndrome

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

The Alagille syndrome (arteriohepatic dysplasia).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Alagille syndrome and deletion of 20p.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Syndrome of intrahepatic biliary dysgenesis and cardiovascular malformations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Anterior chamber cleavage syndrome. A stepladder classification.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Studies of the aetiology of neonatal hepatitis and biliary atresia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Del(20p) with manifestations of arteriohepatic dysplasia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050372

Arteriohepatic Dysplasia: A Benign Syndrome of Intrahepatic Cholestasis with Multiple Organ Involvement

30 October 2018

1 reference

12 December 2020

Arteriohepatic dysplasia: radiologic features of a new syndrome

1 reference

12 December 2020

Arteriohepatic dysplasia: phenotypic features and family studies

1 reference

12 December 2020

Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members

1 reference

12 December 2020

Arteriohepatic dysplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Long-term complications of arteriohepatic dysplasia

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.32.4.264

1 reference

28 July 2017

1 reference

28 July 2017

1 reference