Search Results - "Mostacci, C"

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  1. 1

    Analysis of the DNA replication pattern of a translocation (tX/X, qter----p221::p223----qter) chromosome in leukocyte and fibroblast cultures by Pelliccia, F, Ferraro, M, Mostacci, C, de Capoa, A

    Published in Human genetics (01-01-1984)
    “…The results of a detailed analysis of DNA replication in a late replicating tX/X chromosome (qter---p221::p223---qter) are reported. The chronology of DNA…”
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  2. 2

    Ag staining of the nucleolus organizer (NO) and its relationship to satellite association by de Capoa, A, Ferraro, M, Menendez, F, Mostacci, C, Pelliccia, F, Rocchi, A

    Published in Human genetics (01-01-1978)
    “…The frequency of involvement in satellite association and the frequency of selective staining of the secondary constrictions with silver solutions have been…”
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  3. 3

    Characterization of normal and rearranged human chromosomes by simultaneous Q- and R-banding with chromomycin A3 by Mostacci, C, Ferraro, M, Pelliccia, F, Archidiacono, N, Rocchi, M, de Capoa, A

    Published in Cytogenetics and cell genetics (1980)
    “…Simultaneous Q- and R-type banding patterns in human chromosomes have been achieved by staining with chromomycin A3. Some peculiarities of these patterns as…”
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  4. 4

    Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations by Ferraro, M, De Capoa, A, Mostacci, C, Pelliccia, F, Zulli, P, Baldini, M A, Di Nisio, Q

    Published in Journal of medical genetics (01-12-1980)
    “…Chromosome analysis by Q, R, and C banding was performed in a case diagnosed clinically as gonadal dysgenesis and the karyotype was shown to be 46,X,Xt(qter…”
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  5. 5

    Screening for cytogenetic polymorphisms in a random sample of liveborn infants from Italian population by Belloni, G, Benincasa, A, Bosi, A, de Capoa, A, Di Castro, M, Ferraro, M, Lombardi, D, Mostacci, C, Pelliccia, F, Prantera, G

    Published in Acta anthropogenetica (1983)
    “…The frequency of major and minor chromosome variants is studied in a random sample of newborns in Central Italy. Special attention is paid to the objective…”
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