Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study-Reference-Cited by-同舟云学术

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Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study

Published:2022-06-09 Issue:3 Volume:93 Page:720-724
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Shahid Rabia,Yasin Muhammad,Rehman Zia Ur,Jadoon Humaira,Tahir Haleema,Meraj Neelam,Khan Niamat,Zubair Maria,Zulfiqar Irba,Nowshid Maha,Azeem Arfa,Jabeen Musarrat,Hameed Abdul,Saleha Shamim

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

https://www.nature.com/articles/s41390-022-02128-2.pdf

Reference48 articles.

1. Hagerman, R. J. & Hagerman, P. J. Fragile X Syndrome: Diagnosis, Treatment, and Research (Taylor & Francis US, 2002).

2. Omar, H. A. H., Kamal, T. M., Abd-Alkhalek, H. S., El Nady, G. H. & Salem, M. Molecular characterization of X chromosome fragility in idiopathic mental retardation. Egyptian. J. Med. Hum. Genet. 17, 165–172 (2016).

3. Wheeler, A., Raspa, M., Bishop, E. & Bailey, D. Jr Aggression in fragile X syndrome. J. Intellect. Disabil. Res. 60, 113–125 (2016).

4. Brackett, D. M. et al. FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain. PloS One 8, e58296 (2013).

5. Alvarez-Mora, M. I. et al. Paternal transmission of a FMR1 full mutation allele. Am. J. Med. Genet. Part A 173, 2795–2797 (2017).

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