| scholarly article | Q13442814 |
| P50 | author | Danuta Z Loesch | Q91179403 |
| Yoshimi Inaba | Q123050466 | ||
| Howard R Slater | Q123050473 | ||
| Elsdon Storey | Q5367479 | ||
| Randi J. Hagerman | Q25324810 | ||
| Minh Bui | Q39063603 | ||
| David J Amor | Q49749558 | ||
| Glynda J. Kinsella | Q50255147 | ||
| David E Godler | Q56996913 | ||
| P2093 | author name string | Michele Y Ono | |
| John L Hopper | |||
| David Francis | |||
| Freya Gehling | |||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cognitive dysfunction | Q57859955 |
| P304 | page(s) | 590-598 | |
| P577 | publication date | 2012-01-10 | |
| P1433 | published in | Clinical Chemistry | Q849687 |
| P1476 | title | Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study | |
| P478 | volume | 58 |
| Q50307879 | A pilot proteomic study of protein markers in autism spectrum disorder |
| Q90950470 | Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing |
| Q28087781 | Advanced technologies for the molecular diagnosis of fragile X syndrome |
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| Q37622638 | Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females. |
| Q46017813 | Clinical and molecular correlates in fragile X premutation females. |
| Q36811538 | Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis |
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| Q92262657 | Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome |
| Q50301216 | Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X. |
| Q92192968 | Mass Spectrometry for the Study of Autism and Neurodevelopmental Disorders |
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| Q89031590 | Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction |
| Q34544358 | Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert |
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