Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique
in: Human genetics , ISSN 1432-1203, Vol. 31 (3. 1976), p. 315-328 Zugang:
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1976
Summary Chromosome analysing using quinacrine fluorescence was performed on 930 consecutive newborn infants. The total incidence of major chromosome aberrations including numerical changes of the sex chromosomes, and structural changes of autosomes, was 0.54%. Incidences of XYY (0.4%) and XXY... mehr
Population structure, differential bias and genomic control in a large-scale, case-control association study
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 37, No. 11 (2005), p. 1243-1246 Zugang:
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2005
The main problems in drawing causal inferences from epidemiological case-control studies are confounding by unmeasured extraneous factors, selection bias and differential misclassification of exposure. In genetics the first of these, in the form of population structure, has dominated recent... mehr
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 7 (2007), p. 857-864 Zugang:
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2007
The Wellcome Trust Case Control Consortium (WTCCC) primary genome-wide association (GWA) scan on seven diseases, including the multifactorial autoimmune disease type 1 diabetes (T1D), shows associations at P < 5 × 10−7 between T1D and six chromosome regions: 12q24, 12q13, 16p13, 18p11, 12p13... mehr
The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 409, No. 6822 (2001), p. 942-943 Zugang:
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2001
We constructed maps for eight chromosomes (1, 6, 9, 10, 13, 20, X and (previously) 22), representing one-third of the genome, by building landmark maps, isolating bacterial clones and assembling contigs. By this approach, we could establish the long-range organization of the maps early in the... mehr
The DNA sequence of human chromosome 22
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 402, No. 6761 (1999), p. 489-495 Zugang:
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1999
Knowledge of the complete genomic DNA sequence of an organism allows asystematic approach to defining its genetic components. The genomic sequenceprovides access to the complete structures of all genes, including those withoutknown function, their control elements, and, by inference, the proteins... mehr
American Society of Colon and Rectal Surgeons 91st Annual Convention Podium and Poster abstracts
in: Diseases of the colon & rectum , ISSN 1530-0358, Vol. 35 (5. 1992), p. P1 Zugang:
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1992
Copyright: Copyright 1992 American Society of Colon and Rectal Surgeons mehr
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