Familial growth and skeletal features associated with SHOX haploinsufficiency.

Munns, C F J; Glass, I A; Flanagan, S; Hayes, M; Williams, B; Berry, M; Vickers, D; O'Rourke, P; Rao, E; Rappold, G A; Hyland, V J; Batch, J A

Munns, C F J; Glass, I A; Flanagan, S; Hayes, M; Williams, B; Berry, M; Vickers, D; O'Rourke, P; Rao, E; Rappold, G A; Hyland, V J; Batch, J A.

Affiliation

Munns CF; Endocrine and Diabetes Research Unit, Royal Children's Hospital Foundation Research Centre, Department of Paediatrics and Child Health, University of Queensland, Brisbane, Australia. cmunns@shriners.mcgill.ca

J Pediatr Endocrinol Metab ; 16(7): 987-96, 2003 Sep.

Article in En | MEDLINE | ID: mdl-14513875

Subject(s)

Bone Development/genetics; Growth Disorders/genetics; Growth/genetics; Homeodomain Proteins/genetics; Adolescent; Adult; Age Determination by Skeleton; Aged; Arm/anatomy & histology; Arm/growth & development; Body Height/genetics; Body Height/physiology; Bone Density/genetics; Bone Density/physiology; Bone and Bones/diagnostic imaging; Child; Cohort Studies; Female; Genotype; Haplotypes; Humans; Infant, Newborn; Leg/anatomy & histology; Leg/growth & development; Male; Middle Aged; Pedigree; Phenotype; Short Stature Homeobox Protein; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Bone Development / Homeodomain Proteins / Growth / Growth Disorders Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged / Newborn Language: En Journal: J Pediatr Endocrinol Metab Journal subject: ENDOCRINOLOGIA / PEDIATRIA Year: 2003 Type: Article Affiliation country: Australia

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