(Q34434836)

2 August 2017

The gene encoding I-mf (Mdfi) maps to human chromosome 6p21 and mouse chromosome 17. (English)

1 reference

2 August 2017

Kraut N

1

1 reference

2 August 2017

1 August 1997

1 reference

2 August 2017

2

1 reference

based on heuristic

inferred from page(s)

published in

Mammalian Genome

1 reference

2 August 2017

8

1 reference

2 August 2017

8

1 reference

2 August 2017

618-619

1 reference

https://scigraph.springernature.com/pub.10.1007/s003359900517

2 August 2017

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

I-mf, a novel myogenic repressor, interacts with members of the MyoD family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

The MyoD family and myogenesis: redundancy, networks, and thresholds

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

A Gene Map of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

Animal model: skeletal anomalies in mice with cleidocranial dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900517

A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9250874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S003359900517

1 reference

2 August 2017

1 reference

PubMed ID

9250874