(Q70795656)

English

Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13)

scientific article published on 01 January 1981

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13) (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

A Schinzel

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1981

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

56

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

263-268

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239509

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239509

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239509

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239509

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inverted tandem (“mirror”) duplications in human chromosomes: Inv dup 8p, 4q, 22q

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239509

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00274676

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239509%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

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