Osteoglophonic dysplasia: A 'common' mutation in a rare disease

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Bibliographic Details
Published in:	Clinical genetics Vol. 78; no. 2; pp. 197 - 198
Main Authors:	Sow, AJ, Ramli, R, Latiff, ZA, Ichikawa, S, Gray, AK, Nordin, R, Abd Jabar, MN, Primuharsa Putra, SHA, Siar, CH, Econs, MJ
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01-08-2010 Wiley-Blackwell
Subjects:	Adolescent Base Sequence Biological and medical sciences Child, Preschool DNA Mutational Analysis Dwarfism - genetics Exons - genetics Facies Female Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genetics of eukaryotes. Biological and molecular evolution Heterozygote Humans Medical genetics Medical sciences Molecular and cellular biology Molecular Sequence Data Mutation - genetics Receptor, Fibroblast Growth Factor, Type 1 - genetics Human Genetics Dysplasia Mutation Rare disease
Online Access:	Get full text
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Bibliography:	ArticleID:CGE1382 istex:3AD593CECA0D513C26A2AEBBBCCC5D868DD70E0C ark:/67375/WNG-S8SQ5RFZ-V ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0009-9163 1399-0004
DOI:	10.1111/j.1399-0004.2010.01382.x