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Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome.

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第一作者: Indraneel,Banerjee
第一单位: Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK.
作者单位: Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK. [1] Department of Paediatric Endocrinology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK. [2] Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK. [3] Institute of Human Genetics, University Hospital, Otto-von-Guericke University, Magdeburg, Germany. [4] Department of Paediatrics, University Hospital, Otto-von-Guericke University, Magdeburg, Germany. [5] Department of Paediatric Endocrinology, Royal Victoria Infirmary, Newcastle, UK. [6] Department of Paediatric Endocrinology & Diabetes, Royal Alexandra Children's Hospital, Brighton, UK. [7] Department of Paediatrics and Adolescent Medicine, Ulm University Hospital, Ulm, Germany. [8] Northern Genetics Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK. [9] Department of Pediatric Endocrinology, Ankara University School of Medicine, Ankara, Turkey. [10] Department for Children and Adolescent Medicine, HELIOS Vogtland-Klinikum Plauen, Plauen, Germany. [11] Endocrinology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK. [12] Department of Endocrinology, Sydney Children's Hospital, Randwick and School of Women's and Children's Health,, Sydney, New South Wales, Australia. [13] Department of Pediatric Medicine, Sidra Medicine, Doha, Qatar. [14]
DOI 10.12688/wellcomeopenres.15465.2
PMID 32832699
发布时间 2024-03-29
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Wellcome open research

Wellcome open research

2019年4卷

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