dc.contributor.author | Schaefer, Franz | |
dc.contributor.author | Burgmaier, Kathrin | |
dc.contributor.author | Brinker, Leonie | |
dc.contributor.author | Erger, Florian | |
dc.contributor.author | Beck, Bodo | |
dc.contributor.author | Benz, Marcus | |
dc.contributor.author | Bergmann, Carsten | |
dc.contributor.author | Uetz, Barbara | |
dc.contributor.author | Weber, Lutz T. | |
dc.contributor.author | Wuehl, Elke | |
dc.contributor.author | Zerres, Klaus | |
dc.contributor.author | Doetsch, Joerg | |
dc.contributor.author | Liebau, Max Christoph | |
dc.contributor.author | Boyer, Olivia | |
dc.contributor.author | Collard, Laure | |
dc.contributor.author | Dafinger, Claudia | |
dc.contributor.author | Fila, Marc | |
dc.contributor.author | Kowalewska, Claudia | |
dc.contributor.author | Lange-sperandio, Barbel | |
dc.contributor.author | Massella, Laura | |
dc.contributor.author | Mastrangelo, Antonio | |
dc.contributor.author | Mekahli, Djalila | |
dc.contributor.author | Miklaszewska, Monika | |
dc.contributor.author | Ortiz-Bruechle, Nadina | |
dc.contributor.author | Patzer, Ludwig | |
dc.contributor.author | Prikhodina, Larisa | |
dc.contributor.author | Ranchin, Bruno | |
dc.contributor.author | Ranguelov, Nadejda | |
dc.contributor.author | Schild, Raphael | |
dc.contributor.author | Seeman, Tomas | |
dc.contributor.author | Sever, Lale | |
dc.contributor.author | Sikora, Przemyslaw | |
dc.contributor.author | Szczepanska, Maria | |
dc.contributor.author | Teixeira, Ana | |
dc.contributor.author | Thumfart, Julia | |
dc.date.accessioned | 2021-12-10T13:07:20Z | |
dc.date.available | 2021-12-10T13:07:20Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Burgmaier K., Brinker L., Erger F., Beck B., Benz M., Bergmann C., Boyer O., Collard L., Dafinger C., Fila M., et al., "GENOTYPE-PHENOTYPE CORRELATIONS IN 304 PATIENTS WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) AND PKHD1 VARIANTS", PEDIATRIC NEPHROLOGY, cilt.36, sa.10, ss.3348-3349, 2021 | |
dc.identifier.issn | 0931-041X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_efff58a5-d576-4044-91b0-236d406bbe15 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/175459 | |
dc.language.iso | eng | |
dc.subject | Pediatrics | |
dc.subject | Health Sciences | |
dc.subject | Pediatrics, Perinatology and Child Health | |
dc.subject | Urology | |
dc.subject | İç Hastalıkları | |
dc.subject | Nefroloji | |
dc.subject | Nephrology | |
dc.subject | PEDİATRİ | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | ÜROLOJİ VE NEFROLOJİ | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.title | GENOTYPE-PHENOTYPE CORRELATIONS IN 304 PATIENTS WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) AND PKHD1 VARIANTS | |
dc.type | Makale | |
dc.relation.journal | PEDIATRIC NEPHROLOGY | |
dc.contributor.department | University of Cologne , , | |
dc.identifier.volume | 36 | |
dc.identifier.issue | 10 | |
dc.identifier.startpage | 3348 | |
dc.identifier.endpage | 3349 | |
dc.contributor.firstauthorID | 2740861 | |