(Q66972938)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

title

Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations (English)

1 reference

human chromosomes 6-12 and X

17 June 2023

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

8 July 2022

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

chromosomal translocation

8 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

8 July 2022

1 reference

17 June 2023

author name string

H. Nakai

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

8 July 2022

Y. Yamamoto

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

8 July 2022

Y. Kuroki

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A511169

8 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=511169

8 July 2022

publication date

1 October 1979

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

2 October 1979

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=511169

full work available at URL

8 July 2022

http://link.springer.com/content/pdf/10.1007/BF00283408.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00283408/fulltext.html

17 June 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00283408

17 June 2023

1 reference

17 June 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

1 September 2019

page(s)

349-355

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00283408

1 September 2019

exact match

0 references

cites work

The problem of partial trisomy 22 reconsidered

1 reference

12 December 2020

A (17;22) translocation, balanced, 46 chromosomes. Repository identification No. GM-119

1 reference

12 December 2020

Partial trisomy 22: a recognizable syndrome

1 reference

12 December 2020

The problem of trisomy 22. A case report and a discussion of the variant forms

1 reference

12 December 2020

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy

1 reference

12 December 2020

Trisomy 11q. Individualization of a new syndrome

1 reference

12 December 2020

Cat eye syndrome. Partial trisomy 22 due to translocation in the mother

1 reference

12 December 2020

An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat

1 reference

12 December 2020

47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22

1 reference

12 December 2020

Letter: Satellite staining of human chromosomes

1 reference

12 December 2020

Trisomy 22: A clinical entity

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00283408

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:511169%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 September 2019

0 references

1 reference