Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype

被引：0
|
作者：
S. E. Flanagan
D. J. G. Mackay
S. A. W. Greeley
T. J. McDonald
V. Mericq
J. Hassing
E. J. Richmond
W. R. Martin
C. Acerini
A. M. Kaulfers
D. P. Flynn
J. Popovic
M. A. Sperling
K. Hussain
S. Ellard
A. T. Hattersley
机构：
[1] University of Exeter Medical School,Kovler Diabetes Center
[2] Wessex Regional Genetics Laboratory,Institute of Maternal and Child Research, Faculty of Medicine
[3] Salisbury District Hospital,Pediatric Endocrinology
[4] The University of Chicago,Department of Paediatrics
[5] University of Chile,Pediatric Endocrinology
[6] Pediatric Endocrinology,Division of Pediatric Endocrinology, Children’s Hospital of Pittsburgh of UPMC
[7] Rockwood Clinic,Department of Endocrinology
[8] Pediatric Endocrinology,The Institute of Child Health
[9] National Children’s Hospital,undefined
[10] Sacred Heart Children’s Hospital,undefined
[11] University of Cambridge,undefined
[12] University of South Alabama,undefined
[13] University of Pittsburgh School of Medicine,undefined
[14] Great Ormond Street Hospital for Children NHS Trust,undefined
[15] University College London,undefined
来源：
Diabetologia | 2013年 / 56卷
关键词：
Chromosome 6q24; Hypoglycaemia; Transient neonatal diabetes mellitus; Uniparental disomy;
D O I：
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学科分类号：
摘要：
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页码：218 / 221
页数：3
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