Pages that link to "Q57943475"
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The following pages link to Fragile X premutations in familial premature ovarian failure (Q57943475):
Displaying 37 items.
- Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene (Q28077015) (← links)
- CGG repeat sizing in the FMR1 gene in Indian women with premature ovarian failure (Q28256605) (← links)
- Studies of FRAXA and FRAXE in women with premature ovarian failure (Q33681082) (← links)
- Premature ovarian failure: etiology and prospects (Q34081134) (← links)
- Premature ovarian failure in the fragile X syndrome (Q34306135) (← links)
- Ovarian aging and premature ovarian failure (Q34330442) (← links)
- Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population (Q34388858) (← links)
- Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes. (Q34699414) (← links)
- Fragile X and other trinucleotide repeat diseases (Q34729091) (← links)
- Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses (Q35144045) (← links)
- Fragile X Premutations Are Not a Major Cause of Early Menopause (Q35250296) (← links)
- A novel assay for evaluating fragile X locus repeats (Q35356435) (← links)
- Mechanisms of follicular dysfunction in 46,XX spontaneous premature ovarian failure (Q35560259) (← links)
- Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors (Q36208811) (← links)
- Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers (Q36237133) (← links)
- Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests (Q36475081) (← links)
- Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women (Q37058031) (← links)
- Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia (Q37117706) (← links)
- Inhibin and premature ovarian failure. (Q37596762) (← links)
- A retrospective chromosome studies among Iranian infertile women: Report of 21 years (Q37615586) (← links)
- Premature ovarian failure: a critical condition in the reproductive potential with various genetic causes (Q37680108) (← links)
- Genetic aspects of premature ovarian failure: a literature review (Q37824277) (← links)
- Fragile X-associated disorders: a clinical overview. (Q37900184) (← links)
- Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles (Q40429123) (← links)
- A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population (Q40715457) (← links)
- Screening for Fragile X Syndrome: Information Needs for Health Planners (Q41579814) (← links)
- FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X. (Q44250695) (← links)
- The Impact of Genetic Variation and Gene Expression Level of The Follicle-Stimulating Hormone Receptor on Ovarian Reserve. (Q47141222) (← links)
- Identification of allelic variants in the follicle-stimulating hormone receptor genes of females with or without hypergonadotropic amenorrhea (Q47719462) (← links)
- Examination of reproductive aging milestones among women who carry the FMR1 premutation (Q48788754) (← links)
- Association between idiopathic premature ovarian failure and fragile X premutation. (Q51978995) (← links)
- Clinical involvement and protein expression in individuals with the FMR1 premutation. (Q52169510) (← links)
- Seventh International Workshop on the Fragile X and X-linked Mental Retardation. (Q53366504) (← links)
- Confirmation of early menopause in fragile X carriers (Q71621164) (← links)
- Premature ovarian failure (Q71808582) (← links)
- Premature ovarian failure due to an unbalanced translocation on the X chromosome (Q73581407) (← links)
- Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: a pilot study (Q77339399) (← links)