(Q68807617)

English

Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of Pi(alpha 1-antitrypsin)

scientific article published on 01 October 1986

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of Pi(alpha 1-antitrypsin) (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

author name string

Y Yamamoto

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

R Sawa

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

N Okamoto

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

A Matsui

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

M Yanagisawa

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

S Ikemoto

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

publication date

1 October 1986

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

74

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

190-192

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00282092

0 references

An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of band 13q21 is compatible with normal phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of the human alpha 1-antitrypsin gene (PI) to 14q31-32.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of de novo chromosome rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distal monosomy 14 not associated with ring formation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of DNA replication of human chromosomes. II. Replication map and replication model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion 14q and pericentric inversion 14

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new, high frequency variant of alpha1-antitrypsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/3490426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282092

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3490426%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q68807617&oldid=1984103852"