(Q67315112)

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reason for deprecated rank

11 September 2019

title

Partial trisomy 11q and familial translocation 11--22 (author's transl) (English)

marking inconsistent with the registered/official identifier/name

1 reference

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human chromosomes 6-12 and X

29 August 2022

main subject

1 reference

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29 August 2022

chromosome abnormality

1 reference

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29 August 2022

trisomy

1 reference

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chromosomal translocation

29 August 2022

1 reference

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29 August 2022

author name string

F. Giraud

1

1 reference

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29 August 2022

J. F. Mattei

2

1 reference

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29 August 2022

M. G. Mattei

3

1 reference

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29 August 2022

R. Bernard

4

1 reference

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29 August 2022

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=1176125

29 August 2022

publication date

1 August 1975

1 reference

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11 September 2019

25 August 1975

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1176125

29 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1176125%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

volume

28

1 reference

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11 September 2019

issue

4

1 reference

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11 September 2019

page(s)

343-347

1 reference

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47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.

11 September 2019

cites work

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus).

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

A new technic of analysis of the human karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

A case with 46, XX, del (11) (q21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

C 11-D 13-translocation in four generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

[Partial trisomy 11q identified by study, with heat controlled denaturation, of the paternal balanced translocation]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1176125

12 December 2020

Identifiers

1 reference