Objective : To explore the incidence of fragile X premutation in patients with idiopathic premature ovarian failure, particularly in the Korean population. Design : A prospective study. Materials and Methods : Eighty-three women affected by idiopathic premature ovarian failure were recruited for this study. Patient with known causes of premature ovarian failure were excluded : cytogenetic abnormalities, prior chemotherapy, prior bilateral oophorectomy. DNA was extracted from peripheral blood. Fragile X (FRAXA) premutation was evaluated by PCR amplification of and Southern blot analysis for FMR1 gene. Results : The FRAXA premutation was detected in three (3.6%) out of 83 patients with idiopathic premature ovarian failure. Conclusion : Th...
Expansion of the CGG trinucleotide repeat in the 5' untranslated region of the fragile X mental reta...
BACKGROUND: In this paper, we review our clinical preimplantation genetic diagnosis (PGD) programme ...
BACKGROUND: X chromosome aberrations have been reported as the cause of extremely skewed X chromosom...
BACKGROUND: Fragile X premutation carriers are at increased risk of premature ovarian failure (POF),...
A total of 106 women affected by premature ovarian failure (POF) were evaluated for fragile X (FRAXA...
Background: The aim of this study is to investigate the prevalence of the fragile X mental retardati...
[Objective]: To study three molecular parameters (number of CGG repeats, X-inactivation ratio, and e...
The loss-of-function mutation of the FMR1 gene due to expansion of the 5' UTR CGG repeat causes the ...
Since only 20% of female fragile X premutation carriers develop premature ovarian failure (POF, i.e....
Background: One of the known causes of ovarian dysfunction is fragile X mental retardation gene 1 (F...
SummaryObjectiveThe fragile X syndrome is the most common form of familial mental retardation. Most ...
FRAXA premutations have been associated with premature ovarian failure (POF) or menopause before the...
Introduction: Chromosome abnormalities contribute to about 10% of cases of premature ovarian insuffi...
Objective: the aim of this study was to evaluate the presence of mutations in the coding region of t...
2nd advanced courseThe FMR1 gene [Xq27.3; MIM*309550] has an unstable region comprised of CGG triple...
Expansion of the CGG trinucleotide repeat in the 5' untranslated region of the fragile X mental reta...
BACKGROUND: In this paper, we review our clinical preimplantation genetic diagnosis (PGD) programme ...
BACKGROUND: X chromosome aberrations have been reported as the cause of extremely skewed X chromosom...
BACKGROUND: Fragile X premutation carriers are at increased risk of premature ovarian failure (POF),...
A total of 106 women affected by premature ovarian failure (POF) were evaluated for fragile X (FRAXA...
Background: The aim of this study is to investigate the prevalence of the fragile X mental retardati...
[Objective]: To study three molecular parameters (number of CGG repeats, X-inactivation ratio, and e...
The loss-of-function mutation of the FMR1 gene due to expansion of the 5' UTR CGG repeat causes the ...
Since only 20% of female fragile X premutation carriers develop premature ovarian failure (POF, i.e....
Background: One of the known causes of ovarian dysfunction is fragile X mental retardation gene 1 (F...
SummaryObjectiveThe fragile X syndrome is the most common form of familial mental retardation. Most ...
FRAXA premutations have been associated with premature ovarian failure (POF) or menopause before the...
Introduction: Chromosome abnormalities contribute to about 10% of cases of premature ovarian insuffi...
Objective: the aim of this study was to evaluate the presence of mutations in the coding region of t...
2nd advanced courseThe FMR1 gene [Xq27.3; MIM*309550] has an unstable region comprised of CGG triple...
Expansion of the CGG trinucleotide repeat in the 5' untranslated region of the fragile X mental reta...
BACKGROUND: In this paper, we review our clinical preimplantation genetic diagnosis (PGD) programme ...
BACKGROUND: X chromosome aberrations have been reported as the cause of extremely skewed X chromosom...