Synthetic combinations of missense polymorphic genetic changes underlying Down syndrome susceptibility

Author:

Jackson Rebecca A.,Nguyen Mai Linh,Barrett Angela N.,Tan Yuan Yee,Choolani Mahesh A.,Chen Ee Sin

Funder

National University Health System (NUHS).

Ministry of Education - Singapore

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

Reference151 articles.

1. Antonarakis SE, Petersen MB, McInnis MG, Adelsberger PA, Schinzel AA, Binkert F et al (1992) The meiotic stage of nondisjunction in Trisomy 21: determination by using DNA polymorphisms. Am J Hum Genet 50:544–550

2. Canfield MA, Honein MA, Yuskiv N, Xing J, Mai CT, Collins JS et al (2006) National estimates and race/ethnic-specific variation of selected birth defects in the US, 1999–2001. Birth Defects Res A Clin Mol Teratol 76:747–756

3. Bianca S (2002) Non congenital heart disease aspects of Down’s syndrome. Images Paediatr Cardiol 4:3–11

4. Fonatsch C (2010) The role of chromosome 21 in hematology and oncology. Genes Chromosomes Cancer 49:497–508

5. Antonarakis SE (1991) Parental origin of the extra chromosome in Trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group. N Engl J Med 324:872–876

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