(Q43841145)

reason for preferred rank

27 November 2017

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

1 reference

15 October 2023

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1150232

autosomal deletion syndrome

15 October 2023

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%3A1150232

15 October 2023

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1150232

15 October 2023

1 reference

15 October 2023

author name string

U. Francke

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1150232

15 October 2023

C. Kernahan

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1150232

15 October 2023

C. Bradshaw

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1150232

15 October 2023

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=1150232

15 October 2023

publication date

1 January 1975

1 reference

full work available at URL

27 November 2017

http://link.springer.com/content/pdf/10.1007/BF00285386.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00285386/fulltext.html

15 October 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00285386

15 October 2023

1 reference

15 October 2023

1 reference

27 November 2017

26

1 reference

27 November 2017

343-351

1 reference

27 November 2017

4

1 reference

A Case of?6p- Chromosomal Aberration

27 November 2017

1 reference

12 December 2020

[New system of chromosome banding: the T bands (author's transl)]

1 reference

12 December 2020

[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME.]

1 reference

12 December 2020

C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations

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

Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12

1 reference

12 December 2020

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations

1 reference

12 December 2020

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]

1 reference

12 December 2020

Brother and sister with trisomy 10p: a new syndrome

1 reference

12 December 2020

46, Del (9) (22:), a new deletion syndrome

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

Identifiers

DOI

10.1007/BF00285386

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1150232

15 October 2023

1 reference