(Q55061889)

16 June 2018

reason for preferred rank

title

Probable pericentric inversion in chromosome No. 1 in a female child (46,XX,inv(Ip+q-)) (English)

1 reference

19 May 2023

Probable pericentric inversion in chromosome no. 1 in a female child (46,XX,inv(Ip+q-) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 2023

main subject

human chromosomes 1-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 2023

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 2023

1 reference

19 May 2023

author name string

A. V. Mikelsaar

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 2023

E. V. Ananjev

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 2023

V. M. Gindilis

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5449945

19 May 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=5449945

19 May 2023

publication date

1 January 1970

1 reference

16 June 2018

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00286996.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00286996/fulltext.html

19 May 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00286996

19 May 2023

1 reference

19 May 2023

1 reference

16 June 2018

volume

9

1 reference

16 June 2018

issue

4

1 reference

16 June 2018

page(s)

316-324

1 reference

16 June 2018

Enlarged chromosome No. 1 in a patient with primary amenorrhoea

cites work

1 reference

12 December 2020

Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter

1 reference

12 December 2020

A large deletion of chromosome no. 1 (46,XY,1?--)

1 reference

12 December 2020

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome

1 reference

12 December 2020

Heterochromatisation as a change of chromosome cycle

1 reference

12 December 2020

A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION

1 reference

12 December 2020

[Cytogenetic study of a mother and her son presenting the same ocular malformation]

1 reference

12 December 2020

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00286996

1 reference

16 June 2018

1 reference

16 June 2018