(Q69643720)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

reason for deprecated rank

4 October 2019

title

T�trasomie partielle du chromosome 9, � l'�tat de mosa�que, chez un enfant porteur de malformations multiples (French)

marking inconsistent with the registered/official identifier/name

1 reference

reason for deprecated rank

3 March 2023

Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl) (English)

marking inconsistent with the registered/official identifier/name

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4772080

human chromosomes 6-12 and X

3 March 2023

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4772080

3 March 2023

1 reference

3 March 2023

author name string

D. Ghymers

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4772080

3 March 2023

B. Hermann

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4772080

3 March 2023

C. Distèche

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4772080

3 March 2023

J. Frederic

4

1 reference

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3 March 2023

language of work or name

French

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4772080

3 March 2023

publication date

1 December 1973

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

10 December 1973

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4772080

full work available at URL

3 March 2023

http://link.springer.com/content/pdf/10.1007/BF00385740.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00385740/fulltext.html

3 March 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00385740

3 March 2023

1 reference

3 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

page(s)

273-282

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

Chemical differentiation along metaphase chromosomes

4 October 2019

cites work

1 reference

12 December 2020

On three cases of C trisomy

1 reference

12 December 2020

Pericentric inversion of chromosome 9.

1 reference

12 December 2020

New technique for distinguishing between human chromosomes

1 reference

12 December 2020

Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son.

1 reference

12 December 2020

8-Trisomy in the bone marrow. Report of two cases

1 reference

12 December 2020

An analysis of the technical variables in the production of C bands

1 reference

12 December 2020

The sites and relative frequencies of secondary constrictions in human somatic chromosomes

1 reference

12 December 2020

Pericentric inversions of chromosome 9 in two families

1 reference

12 December 2020

4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity

1 reference

12 December 2020

A familial variant of chromosome 9

1 reference

12 December 2020

Detailed recordings of distribution curves of the fluorescence of human chromosomes, by a new application of microdensitometry

1 reference

12 December 2020

Two observations of identical breakages in the same group C chromosome

1 reference

12 December 2020

Pericentric inversion of a group C autosome: a study of three families

1 reference

12 December 2020

A case of break of C chromosome

1 reference

12 December 2020

A group-C ring chromosome in a mentally deficient male

1 reference

12 December 2020

A new technic of analysis of the human karyotype

1 reference

12 December 2020

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

12 December 2020

Polymorphism of Human Constitutive Heterochromatin

1 reference

12 December 2020

Identification of a C6-G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus.

1 reference

12 December 2020

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation

1 reference

12 December 2020

Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation

1 reference

12 December 2020

46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies

1 reference

12 December 2020

Non-Identity of Apparently Similar Chromosome Aberrations in Human Lymphoblastoid Cell Lines

1 reference

12 December 2020

Familial transmission of an unusual variant of a group C chromosome

1 reference

12 December 2020

A simplified method of demonstrating Giemsa-Band pattern in human chromosomes

1 reference

12 December 2020

Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

1 reference

12 December 2020

The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man

1 reference

12 December 2020

Cp trisomy: a new syndrome

1 reference

12 December 2020

Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+

1 reference

12 December 2020

[Cytological aspect and intranuclear localization of the heterochromatic segments of C9 chromosomes in man].

1 reference

12 December 2020

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.

1 reference

12 December 2020

Localization of heterochromatin in human chromosomes.

1 reference

12 December 2020

Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

1 reference

12 December 2020

Malignant lymphoma characterized by trisomy C

1 reference

12 December 2020

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques

1 reference

12 December 2020

Preferential breakage of sensitive regions of human chromosomes.

1 reference

12 December 2020

High frequency of a specific chromosome abnormality in leukocytes of a normal female

1 reference

12 December 2020

Specific cytological recognition of the heterochromatic segment of number 9 chromosome in man

1 reference

12 December 2020

Partial C trisomy through translocation t(Cp-;Gp-)

1 reference

12 December 2020

Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9

1 reference

12 December 2020

De Lange Syndrome: Report of a Case with an Unusual Karyotype.

2

1 reference

3 March 2023

Identifiers

DOI

10.1007/BF00385740

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4772080%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1 reference