Cargando…
Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities
Recurrent miscarriages occur in about 5% of couples trying to conceive. In the past decade, the products of miscarriage have been studied using array comparative genomic hybridization (a-CGH). Within the last decade, an association has been proposed between miscarriages and single or multigenic chan...
Autores principales: | Najafi, Kimia, Mehrjoo, Zohreh, Ardalani, Fariba, Ghaderi-Sohi, Siavash, Kariminejad, Ariana, Kariminejad, Roxana, Najmabadi, Hossein |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997959/ https://www.ncbi.nlm.nih.gov/pubmed/33772059 http://dx.doi.org/10.1038/s41598-021-86309-9 |
Ejemplares similares
-
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases
por: Najafi, Kimia, et al.
Publicado: (2019) -
Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages
por: Behjati, Farkhondeh, et al.
Publicado: (2011) -
Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum
por: Kariminejad, Ariana, et al.
Publicado: (2016) -
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis
por: Najafi, Kimia, et al.
Publicado: (2017) -
Investigation of Chromosomal Abnormalities and Microdeletion/
Microduplication(s) in Fifty Iranian Patients with Multiple
Congenital Anomalies
por: Mohammadzadeh, Akbar, et al.
Publicado: (2019)