Author:
Zhang Jingjing,Wu Maoqing,Wang Shixuan,Shah Jagesh V.,Wilson Patricia D.,Zhou Jing
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference32 articles.
1. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology;Zerres;Am. J. Med. Genet.,1998
2. Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD);Adeva;Medicine,2006
3. The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1–p12: implications for genetic counseling;Guay-Woodford;Am. J. Hum. Genet.,1995
4. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein;Ward;Nat. Genet.,2002
5. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats;Onuchic;Am. J. Hum. Genet.,2002
Cited by
33 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献