Search Results - Bernardl, F.

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  1. 1
    A new disease-causing mutation in the GAP-related domain of the NF1 gene

    A new disease-causing mutation in the GAP-related domain of the NF1 gene by Anglani, F., Murgla, A., Bedln, S., Bresin, E., Bernardl, F., Clementi, M., Tenconi, R.

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  2. 2
    Two mutations causing complete androgen insensitivity: a frame-shift in the steroid binding domain and a Cys→Phe substitution in the second zinc finger of the androgen receptor

    Two mutations causing complete androgen insensitivity: a frame-shift in the steroid binding domain and a Cys→Phe substitution in the second zinc finger of the androgen receptor by Baldazzl, L., Baronclnl, C., PIrazzoll, P., Balsamo, A., Capelll, M., Marchettl, G., Bernardl, F., Cacclarl, E.

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  3. 3
    Deletion breakpoints in a 32 bp perfect repeat located 45.1 Kb apart in the human growth hormone gene cluster

    Deletion breakpoints in a 32 bp perfect repeat located 45.1 Kb apart in the human growth hormone gene cluster by Baroncini, C., Baldazzi, L., Pirazzoll, P., Marchetti, G., Capelll, M., Cacclari, E., Bernardl, F.

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  4. 4
    "Analogue Network of Converters": A DFT Technique to Test a Complete Set of ADCs and DACs Embedded in a Complex SiP or SOC

    "Analogue Network of Converters": A DFT Technique to Test a Complete Set of ADCs and DACs Embedded in a Complex SiP or SOC by Kerzerho, V., Cauvet, P., Bernard, S., Azais, F., Comte, M., Renovell, M.

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