Exploring the genetic causes of isolated short stature. What has happened to idiopathic short stature?

Willems, M; Amouroux, C; Barat-Houari, M; Salles, J-P; Edouard, T

Willems, M; Amouroux, C; Barat-Houari, M; Salles, J-P; Edouard, T.

Afiliação

Willems M; Medical Genetic Department for Rare Diseases and Personalised Medicine, Reference Centre AD SOOR, AnDDI-RARE, Competence Centre for Rare Skeletal Disorders, OSCAR Network, Inserm U1298, INM, Arnaud de Villeneuve Hospital and University of Montpellier, Montpellier, France.
Amouroux C; Paediatric Endocrine Unit, Competence Centre for Rare Diseases of Calcium and Phosphate Metabolism, OSCAR Network, Arnaud de Villeneuve Hospital and University of Montpellier, Montpellier, France.
Barat-Houari M; Molecular Biology Unit, Competence Centre for Rare Skeletal Disorders, OSCAR Network, Arnaud de Villeneuve Hospital and University of Montpellier, Montpellier, France.
Salles JP; Endocrine, Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism and Competence Centre for Rare Skeletal Disorders, ERN BOND, OSCAR Network, Children's Hospital, Toulouse University Hospital, Toulouse, France.
Edouard T; Endocrine, Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism and Competence Centre for Rare Skeletal Disorders, ERN BOND, OSCAR Network, Children's Hospital, Toulouse University Hospital, Toulouse, France. Electronic address: edouard.t@chu-toulou

Arch Pediatr ; 28(8S1): 8S27-8S32, 2022 Feb.

Article em En | MEDLINE | ID: mdl-37870530

Palavras-chave

Growth retardation; Idiopathic short stature; Molecular analyses; Skeletal dysplasia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Arch Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

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