Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD) without DNA from an index patient in a current pregnancy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference11 articles.
1. Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1)
2. PKHD1mutations in autosomal recessive polycystic kidney disease (ARPKD)
3. PKHD1mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)
4. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)
5. Milder Presentation of Recessive Polycystic Kidney Disease Requires Presence of Amino Acid Substitution Mutations
Cited by 2 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
1. Autosomal Recessive Polycystic Kidney Disease: A Hepatorenal Fibrocystic Disorder With Pleiotropic Effects;Pediatrics;2014-09-01
2. A rational free energy-based approach to understanding and targeting disease-causing missense mutations;Journal of the American Medical Informatics Association;2013-07
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