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Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia.
Laver, Thomas W; Wakeling, Matthew N; Hua, Janet Hong Yeow; Houghton, Jayne A L; Hussain, Khalid; Ellard, Sian; Flanagan, Sarah E.
Afiliação
  • Laver TW; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Wakeling MN; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Hua JHY; Paediatric Department, Hospital Putrajaya, Putrajaya, Malaysia.
  • Houghton JAL; Department of Molecular Genetics, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
  • Hussain K; Department of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.
  • Ellard S; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Flanagan SE; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Clin Endocrinol (Oxf) ; 89(5): 621-627, 2018 11.
Article em En | MEDLINE | ID: mdl-30238501
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperinsulinismo Congênito Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperinsulinismo Congênito Idioma: En Ano de publicação: 2018 Tipo de documento: Article