(Q39855253)

reason for preferred rank

15 September 2017

title

Trisomy 12p syndrome Evaluation of a family with a t(12;21)(p12.1;p11) translocation with unbalanced offspring (English)

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

15 December 2022

Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

1 reference

human chromosomes 6-12 and X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

chromosomal translocation

15 December 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

15 December 2022

author name string

I. L. Hansteen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

L. Schirmer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

S. Hestetun

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A148983

15 December 2022

language of work or name

1 reference

1 April 1978

1 reference

full work available at URL

15 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1978.tb01190.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1978.tb01190.x/fullpdf

15 December 2022

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

15 December 2022

1 reference

15 September 2017

volume

13

1 reference

15 September 2017

issue

4

1 reference

15 September 2017

page(s)

339-349

1 reference

15 September 2017

cites work

The 12p trisomy syndrome

2

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

Partial trisomy 12p due to t(12;21)pat translocation

15 December 2022

3

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

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

15 December 2022

6

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

15 December 2022

12P trisomy: a syndrome?

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome

15 December 2022

9

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat

15 December 2022

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

12pter to 12p12.2: possible assignment of human triose phosphate isomerase

15 December 2022

17

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

Identification of partial 12 trisomy by quinacrine fluorescence

15 December 2022

19

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1978.TB01190.X

15 December 2022

Identifiers

0 references

1 reference