(Q43541741)

English

Partial monosomy 13 and 21 due to a familial 13/21 translocation

scientific article published in April 1978

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

Partial monosomy 13 and 21 due to a familial 13/21 translocation (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

author name string

P G Otto

1

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

S Toledo

2

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

A Richieri-Costa

3

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

P A Otto

4

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

A M Vianna-Morgante

5

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

S Kasahara

6

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

publication date

1 April 1978

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

41

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Europe PubMed Central

PubMed publication ID

24 November 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

243-250

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

https://scigraph.springernature.com/pub.10.1007/bf00284757

0 references

The G deletion syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A "G" deletion syndrome anti-mongolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of long arms of chromosome 13

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome D (13) associated with multiple congenital malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Chromosomal Syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Resolution of Human Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinoblastoma and D-chromosome deletions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/649151

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00284757

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

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