Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report

BACKGROUND: 9p duplication is a structural chromosome abnormality, described in more than 150 patients to date. In most cases the duplicated segment was derived from a parent being a reciprocal translocation carrier. However, about 15 cases with de novo 9p duplication have been reported previously....

Descripción completa

Detalles Bibliográficos
Autores principales: Amasdl, Saadia, Natiq, Abdelhafid, Elalaoui, Siham Chafai, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868013/
https://www.ncbi.nlm.nih.gov/pubmed/27178284
http://dx.doi.org/10.1186/s13256-016-0830-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868013/
https://www.ncbi.nlm.nih.gov/pubmed/27178284
http://dx.doi.org/10.1186/s13256-016-0830-x

Ejemplares similares