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Pediatric Nephrology

Volumn 12, Issue 6, 1998, Pages 449-451

In utero nephropathy, Denys-Drash syndrome and Potter phenotype

(4) Maalouf, E F a Ferguson, J b Van Heyningen, V b Modi, N a

a HAMMERSMITH HOSPITAL (United Kingdom)

b WESTERN GENERAL HOSPITAL (United Kingdom)

Author keywords

Denys Drash syndrome; Nephropathy; Newborn; Potter phenotype; WT1 mutation

Indexed keywords

DNA; ZINC FINGER PROTEIN;

ARTICLE; CASE REPORT; DENYS DRASH SYNDROME; DNA DETERMINATION; HUMAN; KIDNEY FAILURE; MALE; MISSENSE MUTATION; NEWBORN; POTTER SYNDROME; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ABNORMALITIES, MULTIPLE; ADULT; DNA; FATAL OUTCOME; GENITALIA, MALE; HUMANS; INFANT, NEWBORN; KIDNEY FAILURE, CHRONIC; MALE; MUTATION, MISSENSE; PHENOTYPE; POLYMERASE CHAIN REACTION; SYNDROME;

EID: 0031825745 PISSN: 0931041X EISSN: None Source Type: Journal
DOI: 10.1007/s004670050485 Document Type: Article

Times cited : (13)

References (8)

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2
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3
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5
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.