Louise C Wilson1. Show Affiliations » 1. Clinical & Molecular Genetics Unit, Great Ormond Street Hospital and Institute of Child Health, London, UK. WilsoL@gosh.nhs.uk
Abstract
Entities: Disease Gene
Mesh： See more » AdolescentAdultChildChild, PreschoolChromograninsCohort StudiesFemaleFibrous Dysplasia, Polyostotic/complicationsFibrous Dysplasia, Polyostotic/diagnosisFibrous Dysplasia, Polyostotic/geneticsFrameshift Mutation/geneticsGTP-Binding Protein alpha Subunits, Gs/geneticsGrowthHumansInfantLearning Disabilities/etiologyLearning Disabilities/geneticsMaleMetacarpal Bones/abnormalitiesMetatarsal Bones/abnormalitiesMiddle AgedOssification, Heterotopic/complicationsOssification, Heterotopic/diagnosisOssification, Heterotopic/geneticsPedigreePseudohypoparathyroidism/complicationsPseudohypoparathyroidism/diagnosisPseudohypoparathyroidism/genetics
Substances： See more » ChromograninsGNAS protein, humanGTP-Binding Protein alpha Subunits, Gs
Year: 2006 PMID： 16789633 DOI： 10.1515/jpem.2006.19.s2.671
Source DB: PubMed Journal: J Pediatr Endocrinol Metab ISSN： 0334-018X Impact factor: 1.634