(Q73041355)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

title

A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

author name string

E C Bryda

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

H Ling

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

L Flaherty

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

publication date

1 January 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

number of pages

4

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

1-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1007/S003359900336

A genetic linkage map of the mouse: current applications and future prospects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

A comprehensive genetic map of the mouse genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Towards high resolution maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Chlorambucil-induced mutations in mice recovered in homozygotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

A type VII myosin encoded by the mouse deafness gene shaker-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Simplified mammalian DNA isolation procedure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

High-frequency induction of chromosomal rearrangements in mouse germ cells by the chemotherapeutic agent chlorambucil

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Chlorambucil effectively induces deletion mutations in mouse germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Inherited hearing defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S003359900336

A one-hour procedure for the preparation of genomic DNA from frozen tissues

21 January 2018

1 reference

12 December 2020

H beta 58, an insertional mutation affecting early postimplantation development of the mouse embryo.

1 reference

12 December 2020

A genetic map of the mouse suitable for typing intraspecific crosses

1 reference

12 December 2020

Rapid method for recovery of DNA from agarose gels

1 reference

12 December 2020

A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross

1 reference

12 December 2020

Towards high resolution maps of the mouse and human genomes--a facility for ordering markers to 0.1 cM resolution. European Backcross Collaborative Group

1 reference

12 December 2020

Inherited diseases of the inner ear in man in the light of studies on the mouse

1 reference

12 December 2020

Encyclopedia of the mouse genome V. Mouse chromosome 10

1 reference

12 December 2020

Genetic causes of hearing loss in children.

1 reference

12 December 2020

Identifiers

DOI

10.1007/S003359900336

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9021139 AND SRC:MED&resulttype=core&format=json

31 October 2019

1 reference