Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg201666.pdf
Reference24 articles.
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2. Kelsey G : The hows and whys of imprinting. Trends Genet 2000; 16: 15–16.
3. Knoll JH, Nicholls RD, Magenis RE, Graham Jr JM, Lalande M, Latt SA : Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in the parental origin of the deletion. Am J Med Genet 1989; 32: 285–290.
4. Maher ER, Reik W : Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J Clin Invest 2000; 105: 247–252.
5. Preece MA, Moore GE : Genomic imprinting, uniparental disomy and foetal growth. Trends Endocrinol Metab 2000; 11: 270–275.
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