The perinatal phenotype of Troyer syndrome: Case report and literature review.

Bryson, Lisa; Anderson, Laurie; Pagan, Judith; Hamzollari, Rossella; Hamilton, Mark J

Bryson, Lisa; Anderson, Laurie; Pagan, Judith; Hamzollari, Rossella; Hamilton, Mark J.

Afiliação

Bryson L; West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.
Anderson L; Fetal Medicine Unit, Queen Elizabeth University Hospital, Glasgow, UK.
Pagan J; South East Scotland Clinical Genetics, Western General Hospital, Edinburgh, UK.
Hamzollari R; Glasgow City Health and Social Care Partnership, Children and Families, Drumchapel Health Centre, Glasgow, UK.
Hamilton MJ; West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.

Am J Med Genet A ; 188(12): 3558-3562, 2022 12.

Article em En | MEDLINE | ID: mdl-36135318

Assuntos

Paraplegia Espástica Hereditária; Humanos; Paraplegia Espástica Hereditária/genética; Fenótipo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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