Fragile X premutation carrier screening in Pakistani preconception women in primary care consultation

PURPOSE: Women of reproductive age who carry fragile X premutation (PM) alleles have 56 to 200 CGG repeats in the 5′-untranslated region of FMR1 gene are at increased risk for producing children with intellectual disabilities (ID) or autism spectrum disorders (ASD) due to expansion of PM alleles to...

Descripción completa

Detalles Bibliográficos
Autores principales: Meraj, Neelam, Yasin, Muhammad, Rehman, Zia Ur, Tahir, Haleema, Jadoon, Humaira, Khan, Niamat, Shahid, Rabia, Zubair, Maria, Zulfiqar, Irba, Jabeen, Musarrat, Neelam, Shahzadi, Hameed, Abdul, Saleha, Shamim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895653/
https://www.ncbi.nlm.nih.gov/pubmed/35246105
http://dx.doi.org/10.1186/s12905-022-01632-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895653/
https://www.ncbi.nlm.nih.gov/pubmed/35246105
http://dx.doi.org/10.1186/s12905-022-01632-1

Ejemplares similares