Autosomal dominant polycystic kidney disease: Prenatal diagnosis by DNA analysis and sonography at 14 weeks
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference17 articles.
1. IMPROVED EARLY DIAGNOSIS OF ADULT POLYCYSTIC KIDNEY DISEASE WITH FLANKING DNA MARKERS
2. , , , , , , (1988). Characterization of new probes for diagnosis of polycystic kidney disease (PKD1). In: (Ed.). The Fifth International Clinical Genetic Seminar, New York: Alan R. Liss, 69–76.
3. Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity
4. Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster.
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1. Glomerulocystic disease, a rare cause of renal cysts in infants: A series of three cases;Indian Journal of Pathology and Microbiology;2019
2. Autosomal dominant polycystic kidney disease in children;Current Opinion in Pediatrics;2015-04
3. Renal System;Handbook of Pediatric Autopsy Pathology;2013-04-04
4. Hypertension in Children with Autosomal Dominant Polycystic Kidney Disease (ADPKD);Current Hypertension Reviews;2013-03-01
5. Perinatal Urology;Campbell-Walsh Urology;2012
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