Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders

Clin Genet. 1998 Aug;54(2):152-4. doi: 10.1111/j.1399-0004.1998.tb03719.x.

Authors

G E Hollway¹, J C Mulley

Affiliation

¹ Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, Adelaide, Australia.

PMID: 9761395
DOI: 10.1111/j.1399-0004.1998.tb03719.x

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Amino Acid Substitution
Chromosomes, Human, Pair 4 / genetics
Exons
Genes, Homeobox / genetics*
Genetic Variation / genetics*
Growth Disorders / genetics*
Heteroduplex Analysis
Homeodomain Proteins / genetics*
Humans
Introns
MSX1 Transcription Factor
Polymorphism, Genetic / genetics*
Polymorphism, Single-Stranded Conformational
Sequence Deletion / genetics
Transcription Factors*

Substances

Homeodomain Proteins
MSX1 Transcription Factor
Transcription Factors