Renal-hepatic-pancreatic dysplasia: A broad entity [1]

American Journal of Medical Genetics

Volumn 95, Issue 4, 2000, Pages 399-400

  White, S M ^a   Hurst, J A ^a   Hamoda, H ^b   Chamberlain, P ^c   Bowker, C M ^c  

^a CHURCHILL HOSPITAL   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ASPLENIA; CASE REPORT; DISEASE CLASSIFICATION; DYSPLASIA; FETUS; HUMAN; KIDNEY DYSPLASIA; LETTER; LIVER FIBROSIS; MALE; PRIORITY JOURNAL; SITUS INVERSUS;

ABNORMALITIES, MULTIPLE; CONSANGUINITY; FEMALE; HUMANS; KIDNEY; LIVER; MALE; PANCREAS; PREGNANCY; SYNDROME;

EID: 0034639289     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20001211)95:4<399::AID-AJMG19>3.0.CO;2-9     Document Type: Letter

References (7)

1. Sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia and cysts: A new syndrome?
2. Renal-hepatic-pancreatic dysplasia: A syndrome reconsidered
3. Renal dysplasia and asplenia in two sibs
4. Familial dysplasia of kidneys, liver and pancreas: A probably genetically determined syndrome
5. Cloning of inv, a gene that controls left/right asymmetry and kidney development
6. Renal dysplasia, situs inversus totalis and multisystem fibrosis: A new syndrome
7. Renal-hepatic-pancreatic dysplasia: An autosomal recessive malformation