(Q52107853)

22 April 2018

title

10p- syndrome associated with multiple chromosomal abnormalities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

human chromosomes 6-12 and X

24 July 2022

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

chromosomal deletion syndrome

24 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

author name string

F. Prieto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

L. Badia

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

J. A. Moreno

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

P. Barbero

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 2022

F. Asensi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738725

24 July 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=738725

24 July 2022

publication date

1 December 1978

1 reference

22 April 2018

18 December 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=738725

24 July 2022

1 reference

22 April 2018

volume

45

1 reference

22 April 2018

page(s)

229-235

1 reference

22 April 2018

issue

2

1 reference

22 April 2018

https://scigraph.springernature.com/pub.10.1007/bf00286969

exact match

0 references

cites work

A Case of?6p- Chromosomal Aberration

1 reference

12 December 2020

A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development

1 reference

12 December 2020

Partial deletion of the short arm of chromosome 8

1 reference

12 December 2020

Deletion of the short arm of chromosome No. 10

1 reference

12 December 2020

Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies

1 reference

12 December 2020

Partial deletion of the short arm of the chromosome 9

1 reference

12 December 2020

Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome

1 reference

12 December 2020

A simple technique for demonstrating centromeric heterochromatin

1 reference

12 December 2020

The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Deletion of the short arm of chromosome No. 10.

1 reference

12 December 2020

Autosomal deletions 46,XY,del(12)(p11) and 46,XY-46,XY,del(5)(p13) with no effect on physical or mental development.

1 reference

12 December 2020

Short arm deletion of chromosome 12: report of two new cases

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00286969

1 reference

22 April 2018

1 reference

22 April 2018