Works matching IS 00778923 AND DT 1985 AND VI 450 AND IP 1
Results: 20
A Possible Unitary Genetic Hypothesis for Alzheimer's Disease and Down Syndrome.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 223, doi. 10.1111/j.1749-6632.1985.tb21495.x
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Indications of Centromere Movement during Interphase and Differentiation.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 205, doi. 10.1111/j.1749-6632.1985.tb21494.x
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Mouse Trisomy 16: An Animal Model of Human Trisomy 21 (Down Syndrome).
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 157, doi. 10.1111/j.1749-6632.1985.tb21490.x
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Use of Restriction Fragment Length Polymorphisms to Study the Origin of Human Aneuploidy.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 179, doi. 10.1111/j.1749-6632.1985.tb21492.x
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Molecular Quantitation of Aneuploid Conditions Using Chromosome 21 as a Model.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 85, doi. 10.1111/j.1749-6632.1985.tb21485.x
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Molecular Analysis of Chromosome 21 Using Somatic Cell Hybrids.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 109, doi. 10.1111/j.1749-6632.1985.tb21487.x
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Preface.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. vii, doi. 10.1111/j.1749-6632.1985.tb21477.x
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The Biology of Down Syndrome.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 1, doi. 10.1111/j.1749-6632.1985.tb21478.x
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Genetics of Congenital Heart Malformations: A Stochastic Model.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 191, doi. 10.1111/j.1749-6632.1985.tb21493.x
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Human Chromosome Analysis by Flow Cytometry.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 11, doi. 10.1111/j.1749-6632.1985.tb21479.x
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Molecular Structure and Expression of the Gene Locus on Chromosome 21 Encoding the Cu/Zn Superoxide Dismutase and Its Relevance to Down Syndrome.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 133, doi. 10.1111/j.1749-6632.1985.tb21489.x
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Relating Molecular Specificity to Normal and Abnormal Brain Development.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 239, doi. 10.1111/j.1749-6632.1985.tb21496.x
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Molecular Organization in the Proximal Region of Human Acrocentric Chromosomes.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 55, doi. 10.1111/j.1749-6632.1985.tb21483.x
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Linkage Map on Chromosome 21q and the Association of a DNA Haplotype with a Propensity to Nondisjunction and Trisomy 21.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 95, doi. 10.1111/j.1749-6632.1985.tb21486.x
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Nucleolus Organizing Genes on Chromosome 21: Recombination and Nondisjunction.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 121, doi. 10.1111/j.1749-6632.1985.tb21488.x
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Expression of Genes on Human Chromosome 21.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 43, doi. 10.1111/j.1749-6632.1985.tb21482.x
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Ring Chromosome 21: Characterization of DNA Sequences at Sites of Breakage and Reunion.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 33, doi. 10.1111/j.1749-6632.1985.tb21481.x
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Genetic Linkage Map for Chromosome 21.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 25, doi. 10.1111/j.1749-6632.1985.tb21480.x
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Comparative Gene Mapping of Human Chromosome 21 and Mouse Chromosome 16.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 169, doi. 10.1111/j.1749-6632.1985.tb21491.x
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Localization of Chromosome 21 Probes by in Situ Hybridization.
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- Annals of the New York Academy of Sciences, 1985, v. 450, n. 1, p. 69, doi. 10.1111/j.1749-6632.1985.tb21484.x
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