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

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Veröffentlicht in:Clinical genetics Jg. 54; H. 2; S. 152 - 154
Hauptverfasser: Hollway, Georgina E, Mulley, John C
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Oxford, UK Blackwell Publishing Ltd 01.08.1998
Blackwell
Schlagworte:
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-Zugang:Volltext
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Bibliographie:ark:/67375/WNG-2BMQP8WH-K
istex:60B9F6D87CB8578F55EC1065167BDA8DE2FF9E60
ArticleID:CGE152
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content type line 23
ISSN:0009-9163
1399-0004
DOI:10.1111/j.1399-0004.1998.tb03719.x