Role of lncRNAs in the pathogenic mechanism of human decreased ovarian reserve. [PDF]
Lv Z, Lv Z, Song L, Zhang Q, Zhu S.
europepmc +1 more source
The implications of LncRNAs and premature ovarian insufficiency. [PDF]
Zhao Q +6 more
europepmc +1 more source
Genetic diagnosis of three intellectually disabled individuals in a pedigree and insights into fragile X syndrome diagnosis. [PDF]
Huang J +8 more
europepmc +1 more source
Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation. [PDF]
Protic D +9 more
europepmc +1 more source
Isolated β-Human Chorionic Gonadotropin Elevation-From Pregnancy to Fragile X-associated Premature Ovarian Insufficiency. [PDF]
Sharma PP.
europepmc +1 more source
Aging with the FMR1 Gene: A Life Course Perspective
Fragile X syndrome (FXS) is one of three syndromes identified as a health condition related to fragile X mental retardation (FMR1) gene dysfunction. The other two conditions are Fragile X-associated primary ovarian insufficiency syndrome (FXPOI) and ...
Lieb-Lundell, Cornelia
core
The prevalence of Fragile X - associated disorders in Australia
Fragile X is a group of associated genetic disorders (FXDs) that include: Fragile X Syndrome (FXS) - most common cause of inherited intellectual disability, behavioural disorders and speech and language delays that manifest in early childhood ...
Laurie Brown
core
Personalized Follow Up and Genetic Diagnosis Update of FMR1-Related Conditions: A Change in Diagnosis, Prognosis and Expectations. [PDF]
Roche-Martínez A +5 more
europepmc +1 more source
Optimizing single-session CBT delivery in an 8-session longitudinal therapeutic assessment (FRAX-TA) for women with <i>FMR1</i> Premutation. [PDF]
Montanaro FAM +4 more
europepmc +1 more source
Population-based FMR1 carrier screening among reproductive women. [PDF]
Ain Q +8 more
europepmc +1 more source

