TY  - GEN
AU  - Salimy,Zeinab
AU  - Akbari,Mohammad Taghi
AU  - Deilamani,Faravareh Khordadpoor
TI  - Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency
SN  - 0973-7731
PY  - 2020///1013
KW  - Alleles
KW  - Female
KW  - Fragile X Mental Retardation Protein
KW  - genetics
KW  - Fragile X Syndrome
KW  - diagnosis
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Multilocus Sequence Typing
KW  - Primary Ovarian Insufficiency
KW  - Trinucleotide Repeats
N1  - Publication Type: Journal Article
ER  -