(Q33593782)

28 July 2017

title

Meckel syndrome and neural tube defects in Kuwait (English)

1 reference

28 July 2017

1 reference

1 reference

10.1136/JMG.29.2.140-A

https://api.crossref.org/works/10.1136/JMG.29.2.140-A

15 October 2022

author name string

al Saleh QA

2

1 reference

28 July 2017

A. S. Teebi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1613765

15 October 2022

Q. A. al Saleh

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1613765

15 October 2022

H. Odeh

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1613765

15 October 2022

language of work or name

English

0 references

publication date

1 February 1992

1 reference

full work available at URL

28 July 2017

https://europepmc.org/articles/PMC1015870

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1613765

https://europepmc.org/articles/PMC1015870?pdf=render

15 October 2022

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%3A1613765

https://syndication.highwire.org/content/doi/10.1136/jmg.29.2.140-a

15 October 2022

1 reference

Crossref

DOI

10.1136/JMG.29.2.140-A

https://api.crossref.org/works/10.1136/JMG.29.2.140-A

Journal of Medical Genetics

15 October 2022

published in

1 reference

28 July 2017

volume

29

1 reference

28 July 2017

issue

2

1 reference

28 July 2017

page(s)

140

1 reference

The Meckel syndrome: clinicopathological findings in 67 patients

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=1015870

Meckel syndrome in different populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015870

High incidence of Meckel's syndrome in Gujarati Indians

21 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015870

21 June 2018

12 December 2020

Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015870

Anencephaly: a vanishing problem in Bedouins?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015870

Anencephaly: disappearing in Kuwait?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015870

Phenotypic variability in Meckel-Gruber syndrome

30 October 2018

1 reference

PubMed

12 December 2020

Nonsyndromal anencephaly: possible autosomal recessive variant

1 reference

PubMed

12 December 2020

Phenotypic variation in Meckel syndrome

1 reference

PubMed

12 December 2020

Identifiers

DOI

10.1136/JMG.29.2.140-A

1 reference

28 July 2017

1 reference

28 July 2017

1 reference