Novel heterozygous deletion in the HNF1B-MODY5 gene - Adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and

Conwell, Louise S. and McGown, Ivan P. (2014). Novel heterozygous deletion in the HNF1B-MODY5 gene - Adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and a uterine anomaly. In: APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, (). 29 October-1 November, 2014.

Author Conwell, Louise S.
McGown, Ivan P.
Title of paper Novel heterozygous deletion in the HNF1B-MODY5 gene - Adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and a uterine anomaly
Conference name APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting
Conference location Darwin, NT, Australia
Conference dates 29 October-1 November, 2014
Publication Year 2014
Sub-type Oral presentation
Open Access Status
Language eng
Q-Index Code EX
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Conference Paper
Collection: School of Medicine Publications
 
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Created: Mon, 22 Dec 2014, 12:58:04 EST by Dr Louise Conwell on behalf of Paediatrics & Child Health - RBWH