Search Results - Koppens, Paul F J

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  1. 1
    Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes

    Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes by KOPPENS, Paul F. J, HOOGENBOEZEM, Theo, DEGENHART, Herman J

    Published in Human genetics
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  2. 2
    Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB –TNXA hybrids in apparent large-scale gene conversions

    Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB –TNXA hybrids in apparent large-scale gene conversions by Koppens, Paul F.J., Hoogenboezem, Theo, Degenhart, Herman J.

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  3. 3
    PCR-based detection of CYP21 deletions

    PCR-based detection of CYP21 deletions by Koppens, Paul F J, Degenhart, Herman J

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  4. 4
    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt‐losing congenital adrenal hyperplasia caused by steroid 21‐hydroxylase deficiency

    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt‐losing congenital adrenal hyperplasia caused by steroid 21‐hydroxylase deficien... by Koppens, Paul F. J., Hoogenboezem, Theo, Drop, Stenvert L. S., De Muinck Keizer‐Schrama, Sabine M. P. F., Degenhart, Herman J.

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  5. 5
    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase

    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase by Koppens, Paul F J, Hoogenboezem, Theo, Stenvert L S Drop, Sabine M P F de Muinck

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  6. 6
    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency

    Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficien... by Koppens, Paul F. J., Hoogenboezem, Theo, Drop, Stenvert L. S., De Muinck Keizer-Schrama, Sabine M. P. F., Degenhart, Herman J.

    Published in Clinical Endocrinology
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  7. 7
    Flexible data handling for routine quantitative analyses employing a gas chromatograph-mass spectrometer under computer control

    Flexible data handling for routine quantitative analyses employing a gas chromatograph-mass spectrometer under computer control by Vink, J, Koppens, P C, van Harmelen, F A, van Voorthuijsen, W E

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