(Q46956469)

26 December 2017

title

The 11q-- syndrome: another case report (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

human chromosomes 6-12 and X

3 August 2022

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

3 August 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

chromosomal deletion syndrome

3 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

3 August 2022

author name string

M. T. Mulcahy

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

3 August 2022

J. Jenkyn

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A870416

3 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=870416

3 August 2022

publication date

1 April 1977

1 reference

26 December 2017

15 April 1977

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=870416

3 August 2022

1 reference

26 December 2017

volume

36

1 reference

26 December 2017

page(s)

239-242

1 reference

26 December 2017

issue

2

1 reference

26 December 2017

https://scigraph.springernature.com/pub.10.1007/bf00273264

exact match

0 references

cites work

Anomalies associated with partial deletion of long arm of chromosome 11

1 reference

12 December 2020

Chromosome 11 long arm partial deletion: a new syndrome

1 reference

12 December 2020

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

1 reference

12 December 2020

A case with 46, XX, del (11) (q21)

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00273264

1 reference

26 December 2017

1 reference

26 December 2017