Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology

Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases and has a high infant mortality. Prenatal diagnosis using fetal sonography can be unreliable, especially in early pregnancy. The ARPKD locus has been mapped to proximal chromosome 6p allo...

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Veröffentlicht in:American journal of medical genetics 1998-03, Vol.76 (2), p.137-144
Hauptverfasser: Zerres, Klaus, Mücher, Gabi, Becker, Jutta, Steinkamm, Carsten, Rudnik-Schöneborn, Sabine, Heikkilä, Päivi, Rapola, Juhani, Salonen, Riitta, Germino, Gregory G., Onuchic, Luiz, Somlo, Stefan, Avner, Ellis D., Harman, Leigh A., Stockwin, John M., Guay-Woodford, Lisa M.
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Sprache:eng
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