Perinatal differential diagnosis of cystic kidney disease and urinary tract obstruction: anatomic pathologic, ultrasonographic and genetic findings
- 1 April 2000
- journal article
- review article
- Published by Elsevier in European Journal of Obstetrics & Gynecology and Reproductive Biology
- Vol. 89 (2) , 127-133
- https://doi.org/10.1016/s0301-2115(99)00182-7
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A genetic register for von Hippel-Lindau disease.Journal of Medical Genetics, 1996
- The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24Nature Genetics, 1995
- Management of Prenatally Detected Fetal HydronephrosisMayo Clinic Proceedings, 1995
- A Descriptive Study of Prune Belly in New York State, 1983 to 1989Archives of Pediatrics & Adolescent Medicine, 1995
- Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysisGenomics, 1991
- Prenatal diagnosis and prevention of inherited abnormalities of collagenJournal of Inherited Metabolic Disease, 1989
- Genetics of cystic kidney diseasesPediatric Nephrology, 1987
- Oro‐facio‐digital syndromes I and II: radiological methods for diagnosis and the clinical variationsClinical Genetics, 1984
- Chromosome abnormalities in infants with prune belly anomaly: Association with trisomy 18American Journal of Medical Genetics, 1983
- Frequency of the branchio‐oto‐renal (BOR) syndrome in children with profound hearing lossAmerican Journal of Medical Genetics, 1980