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

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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
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Bibliography:ark:/67375/WNG-2BMQP8WH-K
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ArticleID:CGE152
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0009-9163
1399-0004
DOI:10.1111/j.1399-0004.1998.tb03719.x