(Q41684175)

7 October 2017

The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(qh?,RHG,GAG,CBG) (English)

1 reference

human chromosomes 6-12 and X

21 May 2023

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

1 reference

21 May 2023

author name string

E. Donti

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

G. Venti

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

V. Bocchini

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

G. Rosi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

R. Armellini

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

N. Trabalza

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457134

3 July 2022

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=457134

3 July 2022

publication date

1 April 1979

1 reference

7 October 2017

17 April 1979

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=457134

full work available at URL

3 July 2022

http://link.springer.com/content/pdf/10.1007/BF00273274.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00273274/fulltext.html

21 May 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00273274

21 May 2023

1 reference

21 May 2023

1 reference

7 October 2017

48

1 reference

7 October 2017

53-59

1 reference

7 October 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00273274

7 October 2017

0 references

cites work

Structural variation in human nitotic chromosomes

1 reference

12 December 2020

[Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter]

1 reference

12 December 2020

Radiation-induced non-random chromosome breakage

1 reference

12 December 2020

Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes

1 reference

12 December 2020

High resolution studies on the pattern of induced exchanges in the human karyotype

1 reference

12 December 2020

A specific aberration of a C group chromosome in several members of a family

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

Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia (blackfan-diamond syndrome)

1 reference

12 December 2020

Distribution of spontaneous chromosome breaks in human chromosomes

1 reference

12 December 2020

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

1 reference

12 December 2020

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

12 December 2020

Inherited constriction fragility of chromosome 2.

1 reference

12 December 2020

Two observations of identical breakages in the same group C chromosome

1 reference

12 December 2020

A case of break of C chromosome

1 reference

12 December 2020

Is the chromatid gap a folding defect due to protein change? Evidence from mercaptoethanol treatment of human lymphocyte chromosomes

1 reference

12 December 2020

Familial transmission of an unusual variant of a group C chromosome

1 reference

12 December 2020

A chromosomal break and partial deletion of a number 9 chromosome.

1 reference

12 December 2020

Constitutional chromosomal breakage.

1 reference

12 December 2020

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)

1 reference

12 December 2020

A fragile secondary constriction on chromosome 2 in a severely mentally retarded patient

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

Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect

1 reference

12 December 2020

Persisting clone of cells with an abnormal chromosome in a woman previously irradiated

1 reference

12 December 2020

Preferential breakage of sensitive regions of human chromosomes.

1 reference

12 December 2020

Evidence for an inverse relationship between X-ray induced chromatid and chromosome breakage in human chromosomes

1 reference

12 December 2020

A case of structural aberration of the chromosome A2

1 reference

12 December 2020

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

1 reference

12 December 2020

Structural aberration in chromosome no.2.

1 reference

12 December 2020

[Descriptive diagrams of human chromosomes (R band analysis and nomenclature according to the conference in Paris in 1971)]

1 reference

12 December 2020

Localization of chromatid breaks in Fanconi's anemia, using three consecutive stains

1 reference

12 December 2020

Seasonal variation in the birth of children with aneuploid chromosome abnormalities. Report from the Danish Cytogenetic Central Register

25

1 reference

21 May 2023

Identifiers

DOI

10.1007/BF00273274

1 reference

Dimensions Publication ID

7 October 2017

0 references

1 reference