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

Saved in:

Bibliographic Details
Published in:	Clinical genetics Vol. 54; no. 2; pp. 152 - 154
Main Authors:	Hollway, Georgina E, Mulley, John C
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01.08.1998 Blackwell
Subjects:	Amino Acid Substitution Biological and medical sciences Chromosomes, Human, Pair 4 - genetics craniosynostosis Exons Genes, Homeobox - genetics Genetic Variation - genetics Growth Disorders - genetics Heteroduplex Analysis Homeodomain Proteins - genetics Humans Introns Malformations of the nervous system Medical sciences MSX1 MSX1 Transcription Factor Neurology polymorphism Polymorphism, Genetic - genetics Polymorphism, Single-Stranded Conformational Sequence Deletion - genetics Transcription Factors Genetic mapping Human Nervous system diseases Craniosynostosis Diseases of the osteoarticular system Dysostosis Chromosome B4 Genetic determinism Gene Malformation Skull disease Homeobox sequence Polymorphism
ISSN:	0009-9163, 1399-0004
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!