(Q43814886)

27 November 2017

Concordant congenital malformations in twins with inherited translocation: t(9p--;13q+) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 July 2022

Concordant congenital malformations in twins with inherited translocation: t(9p-;13q+) (English)

1 reference

human chromosomes 6-12 and X

8 June 2023

main subject

congenital disorder

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 July 2022

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

chromosomal translocation

6 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 July 2022

diseases in twins

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 July 2022

1 reference

8 June 2023

author name string

G. S. Sekhon

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 July 2022

K. Taysi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A489011

6 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=489011

6 July 2022

publication date

1 September 1979

1 reference

full work available at URL

27 November 2017

http://link.springer.com/content/pdf/10.1007/BF00399392.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00399392/fulltext.html

8 June 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00399392

8 June 2023

1 reference

8 June 2023

1 reference

27 November 2017

50

1 reference

27 November 2017

271-276

1 reference

27 November 2017

3

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00399392

27 November 2017

0 references

cites work

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

1 reference

12 December 2020

Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12)

1 reference

12 December 2020

Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases

1 reference

12 December 2020

The deletion 9p syndrome. A 61-year-old man with deletion of short arm 9

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00399392

1 reference

Dimensions Publication ID

27 November 2017

0 references

1 reference