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

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Vydané v:	Clinical genetics Ročník 54; číslo 2; s. 152 - 154
Hlavní autori:	Hollway, Georgina E, Mulley, John C
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Oxford, UK Blackwell Publishing Ltd 01.08.1998 Blackwell
Predmet:	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
On-line prístup:	Získať plný text
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