(Q72654477)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

8 July 2023

author name string

G. R. Fraser

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5865628

8 July 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5865628

8 July 2023

publication date

1 November 1965

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

28 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-1809.1965.tb00512.x

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1965.tb00512.x/fullpdf

8 July 2023

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

8 July 2023

published in

Annals of Human Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

volume

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

page(s)

171-196

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

Vestibular function in deafness and severe hardness of hearing.

28 October 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Autoimmunity: some aetiological aspects. Inflammatory polyarthritis and rheumatoid arthritis

8 July 2023

3

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

8 July 2023

A note on deaf mutism

6

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

THE SEX INCIDENCE OF CERTAIN HEREDITARY TRAITS IN MAN

8 July 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

The aetiology of congenital deafness and audiometric patterns.

8 July 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Deafness as part of an hereditary syndrome.

8 July 2023

16

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

PROFOUND CHILDHOOD DEAFNESS.

8 July 2023

18

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

ASSOCIATION OF CONGENITAL DEAFNESS WITH GOITRE (PENDRED'S SYNDROME) A STUDY OF 207 FAMILIES.

8 July 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

8 July 2023

22

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

8 July 2023

31

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

The phenomenon of position effect.

8 July 2023

37

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Gene action in the X-chromosome of the mouse (Mus musculus L.)

8 July 2023

41

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION

8 July 2023

42

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

THE GENETIC MUCOPOLYSACCHARIDOSES

8 July 2023

44

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

8 July 2023

Sex-linked deaf-mutism

58

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

STATISTICAL STUDIES OF THE CHILDREN IN PUBLIC SCHOOLS FOR THE DEAF: ADDITIONAL REPORT OF COMMITTEE, DIVISION OF MEDICAL SCIENCES, NATIONAL RESEARCH COUNCIL

8 July 2023

66

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Hereditary deaf mutism, with particular reference to Northern Ireland

8 July 2023

67

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

DISTINCTION AMONG FOUR FORMS OF HURLER'S SYNDROME

8 July 2023

68

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Audiometric examination of parents of children deaf from birth; the influence of consanguineous marriage.

8 July 2023

78

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

Partial albinism and deaf-mutism due to a recessive sex-linked gene

8 July 2023

82

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1965.TB00512.X

8 July 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5865628%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference