(Q43431827)

English

A survey of a familial transmission of an anomalous autosome in group 13-15.

scientific article published in January 1966

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

A survey of a familial transmission of an anomalous autosome in group 13-15. (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

author name string

S Makino

1

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

J I Muramoto

2

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

S Tabata

3

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

publication date

1 January 1966

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

371-379

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Chromosomal studies in normal human subjects and in 300 cases of congenital disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of human chromosome markers in linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial chromosome abnormality associated with repeated abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MONGOLISM (DOWN'S SYNDROME) WITH ATYPICAL CLINICAL AND CYTOGENETIC FEATURES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies on randomly chosen men and women.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial chromosome translocation associated with speech and mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYTOGENETIC STUDIES IN LEUCOCYTES ON THE GENERAL POPULATION: SUBJECTS OF AGES 65 YEARS AND MORE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4389521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00332543

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

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=Q43431827&oldid=2206033940"