SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome

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Bibliographic Details
Published in:	Clinical genetics Vol. 79; no. 4; pp. 391 - 393
Main Authors:	Suphapeetiporn, K, Srichomthong, C, Shotelersuk, V
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01-04-2011 Wiley-Blackwell
Subjects:	Abnormalities, Multiple - genetics Abnormalities, Multiple - pathology Base Sequence Biological and medical sciences Carrier Proteins - genetics Craniofacial Abnormalities - pathology DNA Mutational Analysis Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genetics of eukaryotes. Biological and molecular evolution Hand Deformities, Congenital - pathology Humans Indexing in process Infant Infant, Newborn Intellectual Disability - pathology Male Medical genetics Medical sciences Molecular and cellular biology Mutation Nails, Malformed - pathology Nuclear Proteins - genetics Thailand Thailand Asia Human Genetics Patient Mutation Thai
Online Access:	Get full text
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Bibliography:	ArticleID:CGE1552 ark:/67375/WNG-42435GZG-Q istex:D54BEA79B0E27C62502B928927B3E8E08B9BFDEE ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23
ISSN:	0009-9163 1399-0004
DOI:	10.1111/j.1399-0004.2010.01552.x