(Q41027658)

25 September 2017

title

Moderate mental retardation and nonspecific dysmorphic syndrome associated with ring chromosome 9 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

moderate mental retardation

4 July 2022

main subject

1 reference

human chromosomes 6-12 and X

inferred from title

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

4 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%3A468257

4 July 2022

1 reference

28 May 2023

author name string

J. P. Fryns

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

4 July 2022

A. Lambrechts

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

4 July 2022

H. Jansseune

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

4 July 2022

H. Van den Berghe

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A468257

4 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=468257

4 July 2022

publication date

1 January 1979

1 reference

full work available at URL

25 September 2017

http://link.springer.com/content/pdf/10.1007/BF00295585.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00295585/fulltext.html

28 May 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00295585

28 May 2023

1 reference

28 May 2023

1 reference

25 September 2017

volume

50

1 reference

25 September 2017

issue

1

1 reference

25 September 2017

page(s)

29-32

1 reference

Partial monosomy of the short arm of chromosome 9: a distinct clinical entity

25 September 2017

cites work

1 reference

12 December 2020

Ring 6-chromosome: a nonspecific clinical picture

1 reference

12 December 2020

Irregular phenotypic expression of ring chromosomes

1 reference

12 December 2020

46,XX/46,XX,r(15) mosaiciam: report of a case

1 reference

12 December 2020

A ring 9 chromosome. Repository identification no. GM-166

1 reference

12 December 2020

A group-C ring chromosome in a mentally deficient male

1 reference

12 December 2020

Mental retardation and congenital malformations associated with a ring chromosome 9.

1 reference

12 December 2020

Two cases with a C-group ring autosome

1 reference

12 December 2020

Ring chromosome 6. Karotype 46, XY, r (6)-45, XY,-6

1 reference

12 December 2020

A chromosomal break and partial deletion of a number 9 chromosome

1 reference

12 December 2020

Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr)

1 reference

12 December 2020

A case of annular chromosome 9. Indentification by controlled denaturation

1 reference

12 December 2020

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

1 reference

12 December 2020

Ring chromosome 9. 46,XY,r(9) in a male with ambiguous external genitalia

1 reference

12 December 2020

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00295585

1 reference

Dimensions Publication ID

25 September 2017

1031807539

0 references

1 reference