(Q33592563)

English

Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome

scientific article published on March 1, 1988

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

congenital disorder

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

1 reference

10.1136/JMG.25.3.204

https://api.crossref.org/works/10.1136/JMG.25.3.204

30 December 2022

author name string

H. Santos

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

J. Mateus

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

M. J. Leal

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

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publication date

1 March 1988

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

full work available at URL

http://jmg.bmjjournals.com/cgi/content/abstract/25/3/204

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3351909/?tool=EBI

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/3351909/pdf/?tool=EBI

Portable Document Format

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1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

https://europepmc.org/articles/PMC1015489

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

https://europepmc.org/articles/PMC1015489?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3351909

30 December 2022

https://syndication.highwire.org/content/doi/10.1136/jmg.25.3.204

1 reference

10.1136/JMG.25.3.204

https://api.crossref.org/works/10.1136/JMG.25.3.204

30 December 2022

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

25

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

204-205

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Waardenburg's syndrome associated with total aganglionosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015489

21 June 2018

Hirschsprung's Disease and Congenital Deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015489

21 June 2018

Meningomyelocele and Hirschprung disease: theoretical and clinical significance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015489

21 June 2018

Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015489

21 June 2018

Neuroblastoma and Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3351909

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.25.3.204

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=3351909

30 December 2022

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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