(Q39828341)

English

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

based on heuristic

inferred from title

author name string

A Hagemeijer

1

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

E M Smit

2

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

publication date

1 August 1977

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

15-23

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00295803

0 references

A case of G-G translocation in tandem

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric human X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple R banding technic

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X).

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four new cases of X-autosome translocation in man (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second example of telomeric fusion 2 X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of G-group chromosomes involved in a G-G tandem-translocation by the giemsa-band technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Two subterminal heterochromatin regions in a rare form of 21-21 translocation]

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human nucleolar organizer chromosomes: satellite associations

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 21 (21q21 - 21q22.2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Down's syndrome: clinical vs. laboratory

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apparently isodicentric but functionally monocentric X chromosome in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Milledgeville mongoloid: a rare karyotype of Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism)

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some general problems of chromosomal evolution and speciation in animals

1 reference

https://pubmed.ncbi.nlm.nih.gov/143443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00295803

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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