Author:
Shaw Sheng-Wen,Chen Chih-Ping,Cheng Po-Jen,Wang Tzu-Hao,Hou Jia-Woei,Lin Cheng-Tao,Chang Shuenn-Dhy,Hwa Hsiao-Lin,Lin Ju-Li,Chao An-Shine,Soong Yung-Kuei,Hsieh Fon-Jou
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference43 articles.
1. International Human Genome Sequencing Consortium (2004) Finishing the euchromatic sequence of the human genome. Nature 431:931–945
2. Antonarakis SE (1998) 10 years of genomics, chromosome 21, and Down syndrome. Genomics 51:1–16
3. Antonarakis SE, Adelsberger PA, Petersen MB, Binkert F, Schinzel AA (1990) Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations. Am J Hum Genet 47:968–972
4. Antonarakis SE, Lyle R, Dermitzakis ET, Reymond A, Deutsch S (2004) Chromosome 21 and down syndrome: from genomics to pathophysiology. Nat Rev Genet 5:725–738
5. Bandyopadhyay R, Heller A, Knox-DuBois C, McCaskill C, Berend SA, Page SL, Shaffer LG (2002) Parental origin and timing of de novo Robertsonian translocation formation. Am J Hum Genet 71:1456–1462
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