(Q45805099)

http://europepmc.org/abstract/PMC/1468592

16 December 2017

title

De Lange Syndrome: Report of a Case with an Unusual Karyotype (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

0 references

J. M. Berg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

G. F. Smith

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

M. A. C. Ridler

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

B. D. McCreary

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

Janet A. Faunch

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

Faith N. Farnham

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

Mary L. Allen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

language of work or name

English

0 references

publication date

1 September 1967

1 reference

http://europepmc.org/abstract/PMC/1468592

16 December 2017

published in

Journal of Medical Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

page(s)

184-189

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

Aneusomie de recombinaison: three further examples

13 May 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

The Cornelia de Lange syndrome: clinical and cytogenetic interpretations

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

TRANSLOCATION IN DE LANGE'S SYNDROME?

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

DE LANGE'S AMSTERDAM DWARFS SYNDROME. A CASE REPORT.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

BRACHMANN/DE LANGE SYNDROME SYNDROME.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

DE LANGE SYNDROME. THE "AMSTERDAM TYPE" OF MENTAL DEFECT WITH CONGENITAL MALFORMATION.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

THE CORNELIA DE LANGE SYNDROME.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468592

15 August 2018

Identifiers

DOI

10.1136/JMG.4.3.184

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC1468592&resulttype=core&format=json

13 May 2020

1 reference