| 1 | CFP, PFD
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| Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
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| van den Bogaard R, Fijen CA, Schipper MG, de Galan L, Kuijper EJ, Mannens MM.
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| Eur J Hum Genet 8(7):513-8. 2000
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| 2 | PFD
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| Carrier detection in families with properdin deficiency by microsatellite haplotyping.
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| Kšlble K, et al.
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| J Clin Invest 91 : 99-102. 1993
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| 3 | PFD
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| Linkage analysis in properdin deficiency families : refined location in proximal Xp.
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| Wadelius C, et al.
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| Clin Genet 42 : 8-12. 1992
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| 4 | CFP, PFD
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| Localization of the properdin structural locus to Xp11.23-Xp21.1.
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| Goundis D, Holt SM, Boyd Y, Reid KB.
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| Genomics 5 : 56-60. 1989
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| 5 | PFD
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| Linkage analysis suggest location of the properdin deficiency gene on the proximal part of the p-arm of the X-chromosome.
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| Wadelius C, et al.
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| (HGM10) Cytogenet Cell Genet 51 : 1100. 1989
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| 6 | PFD
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| Linkage analysis of the properdin deficiency gene : suggestion of a locus in the proximal part of the short arm of the X chromosome.
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| Goonewardena P, et al.
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| Genomics 2 : 115-118. 1988
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| 7 | PFD
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| The locus for properdin deficiency maps within Xp21.1-Xcen.
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| Goonewardena P, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 622. 1987
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