Ngā hua rapu - Melanie Nemitz‐Kliemchen
- E whakaatu ana i te 1 - 1 hua o te 1
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Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes mā Ria Schönauer, Sebastian Baatz, Melanie Nemitz‐Kliemchen, Valeska Frank, Friederike Petzold, Sebastian Sewerin, Bernt Popp, Johannes Münch, Steffen Neuber, Carsten Bergmann, Jan Halbritter
I whakaputaina 2020Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Autosomal dominant polycystic kidney disease
Bioinformatics
Biology
Disease
Exome sequencing
Exon
Gene
Genetic counseling
Genetic heterogeneity
Genetic testing
Genetics
Internal medicine
Medicine
Multiplex ligation-dependent probe amplification
Mutation
Oncology
PKD1
Phenocopy
Phenotype
Polycystic kidney disease