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A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutations.
Lucas-Herald, Angela K; Kinning, Esther; Iida, Aritoshi; Wang, Zheng; Miyake, Noriko; Ikegawa, Shiro; McNeilly, Jane; Ahmed, S Faisal.
Affiliation
  • Lucas-Herald AK; Developmental Endocrinology Research Group (A.K.L.-H., S.F.A.), School of Medicine, University of Glasgow, Royal Hospital for Sick Children (RHSC), Yorkhill, Glasgow, G3 8SJ United Kingdom; Department of Clinical Genetics (E.K.), Southern General Hospital, Glasgow, G51 4TF United Kingdom; Laboratory of Bone and Joint Diseases (A.I., Z.W., S.I.), Center for Integrative Medical Sciences, RIKEN, Tokyo 108-8639, Japan; Department of Human Genetics (N.M.), Yokohama City University Graduate School of
J Clin Endocrinol Metab ; 100(4): 1221-4, 2015 Apr.
Article in En | MEDLINE | ID: mdl-25664603
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carrier Proteins / Human Growth Hormone / Intracellular Signaling Peptides and Proteins / Dwarfism, Pituitary / Mutation Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male Language: En Journal: J Clin Endocrinol Metab Year: 2015 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carrier Proteins / Human Growth Hormone / Intracellular Signaling Peptides and Proteins / Dwarfism, Pituitary / Mutation Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male Language: En Journal: J Clin Endocrinol Metab Year: 2015 Document type: Article