Down's syndrome and the molecular biology of chromosome 21

Author:

Cooper David N.,Hall Christine

Publisher

Elsevier BV

Subject

General Neuroscience

Reference237 articles.

1. Risk for trisomy 21 in offspring of individuals who have relatives with trisomy 21;Abuelo;Am. J. med. Genet.,1986

2. Evidence for genetic control of non-disjunction in man;Alfi;Am. J. hum. Genet.,1980

3. Marker chromosomes in parents to children with Down's syndrome;Annerén;Clin. Genet.,1984

4. Analysis of DNA haplotypes suggest a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21;Antonarakis,1985

5. Reduced recombination rate on chromosomes 21 that have undergone nondisjunction;Antonarakis,1986

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1. Differences in purine metabolism in patients with Down's syndrome;Journal of Intellectual Disability Research;2008-06-28

2. Down's Syndrome: Up-Regulation of β-Amyloid Protein Precursor and τ mRNAs and Their Defective Coordination;Journal of Neurochemistry;2008-06-28

3. Reflections on the pathogenesis of Down syndrome;American Journal of Medical Genetics;2005-06-03

4. Role of oxidative stress in neurodegeneration: recent developments in assay methods for oxidative stress and nutraceutical antioxidants;Progress in Neuro-Psychopharmacology and Biological Psychiatry;2004-08

5. Motoneuronerkrankungen;Erkrankungen des Zentralnervensystems;1999

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