(Q34635152)

3 August 2017

Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques (English)

1 reference

3 August 2017

0 references

Caspersson T

1

1 reference

3 August 2017

Lindsten J

2

1 reference

3 August 2017

Zech L

3

1 reference

3 August 2017

Buckton KE

4

1 reference

3 August 2017

Price WH

5

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 1972

1 reference

Journal of Medical Genetics

3 August 2017

1 reference

3 August 2017

9

1 reference

3 August 2017

1-7

1 reference

3 August 2017

1

1 reference

An Extra C Chromosome and Various Metabolic Abnormalities in the Bone Marrow from a Patient with Refractory Sideroblastic Anaemia

3 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469203

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

7 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469203

[Chromosome mosaicism C-trisomy/normal]

26 October 2018

1 reference

12 December 2020

A further case of presumed 6-12 trisomy

1 reference

12 December 2020

Mosaic Trisomy of an Autosome in the 6–12 Group in a Patient With Multiple Congenital Anomalies

1 reference

12 December 2020

[Frequency of chromosomal aberrations in spontaneous human abortions]

1 reference

12 December 2020

Trisomy C in an infant with polycystic kidneys and other malformations

1 reference

12 December 2020

Apparent C trisomy in bone marrow cells. Report of two cases

1 reference

12 December 2020

Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents

1 reference

12 December 2020

New technique for distinguishing between human chromosomes

1 reference

12 December 2020

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

12 December 2020

Cytogenetic studies in primary amenorrhoea

1 reference

12 December 2020

[Chromosome anomalies in the blood cells of a child with multiple abnormalities]

1 reference

12 December 2020

Identifiers

PMCID

1469203

1 reference

3 August 2017

1 reference