(Q70943627)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

title

Autosomal recessive "uncomplicated" profound childhood deafness in an Arabic family with high consanguinity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Autosomal recessive ?uncomplicated? profound childhood deafness in an arabic family with high consanguinity (English)

1 reference

15 April 2024

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7286990

15 April 2024

1 reference

15 April 2024

author name string

A. Kabarity

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7286990

15 April 2024

S. A. Al-Awadi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7286990

15 April 2024

T. I. Farag

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7286990

15 April 2024

G. Mallalah

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7286990

15 April 2024

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=7286990

15 April 2024

publication date

1 January 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

15 October 2019

http://link.springer.com/content/pdf/10.1007/BF00281704.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00281704/fulltext.html

15 April 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF00281704

15 April 2024

1 reference

15 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

page(s)

444-446

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00281704

15 October 2019

exact match

0 references

cites work

Two types of congenital recessive deafness

1 reference

12 December 2020

A genetic register system (RAPID)

1 reference

12 December 2020

A note on deaf mutism

1 reference

12 December 2020

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

1 reference

12 December 2020

PROFOUND CHILDHOOD DEAFNESS.

1 reference

12 December 2020

DEAF-MUTISM AND GOITRE

16

1 reference

15 April 2024

Identifiers

DOI

10.1007/BF00281704

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7286990%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference