(Q24517832)

10 April 2024

author name string

T. J. David

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

10 April 2024

B. W. Webb

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

10 April 2024

I. R. Gordon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

full work available at URL

10 April 2024

language of work or name

English

0 references

publication date

August 1981

0 references

https://jmg.bmj.com/content/jmedgenet/18/4/294.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%3A7277424

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7277424/pdf/?tool=EBI

10 April 2024

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7277424/?tool=EBI

10 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

http://jmg.bmjjournals.com/cgi/content/abstract/18/4/294

10 April 2024

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%3A7277424

https://europepmc.org/articles/PMC1048735

10 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7277424

https://europepmc.org/articles/PMC1048735?pdf=render

10 April 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%3A7277424

https://syndication.highwire.org/content/doi/10.1136/jmg.18.4.294

10 April 2024

1 reference

https://api.crossref.org/works/10.1136/JMG.18.4.294

Journal of Medical Genetics

10 April 2024

published in

0 references

volume

18

0 references

issue

4

0 references

page(s)

294-8

0 references

cites work

Leprechaunism in a male infant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

DYSTROPHIC CHANGES ASSOCIATED WITH LEPRECHAUNISM IN A MALE INFANT

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

A case of leprechaunism with severe hyperinsulinemia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

A unique chondrodysplasia secondary to a defect in chondroosseous transformation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

27 September 2017

"New" dwarfing syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

Metaphyseal chondrodysplasia calcificans. A report on two cases.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048735

Leprechaunism: a euphemism for a rare familial disorder

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7277424

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Leprechaunism (Donohue's syndrome): Acase report

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7277424

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7277424

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic Disorders Among the Jewish People

https://api.crossref.org/works/10.1136/JMG.18.4.294

11

1 reference

Fairbank's Atlas of General Affections of the Skeleton

10 April 2024

https://api.crossref.org/works/10.1136/JMG.18.4.294

18

1 reference

10 April 2024

Identifiers

0 references

0 references