AIMS: We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) probe set for the detection of aneuploidy to diagnose Turner syndrome (TS). We first fixed an MLPA ratio cutoff able to detect all cases of TS in a pilot TS group. We then tested this value on a second group of TS patients and a short-stature population to measure specificity and sensitivity. METHODS: 15 TS patients with X mosaicism or X structural abnormalities (Pilot TS Group), 45 TS karyotype-assessed patients (TS Group), and 74 prepubertal female patients with apparent idiopathic short stature (Short-Stature Group) were enrolled. All subjects underwent MLPA and karyotype analysis. In the TS and Short-Stature Groups, MLPA testing wa...
The past decade produced important advances in molecular genetic techniques potentially supplanting ...
Abstract Background Ultrasensitive assays to measure pre-pubertal gonadotropins levels could help id...
Abstract Background Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well...
AIMS: We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) ...
Abstract Aims: We aimed at evaluating a standard multiplex ligation-dependent probe amplification (...
Turner syndrome (TS) is one of the most common chromosomal abnormalities among girls. Complete monos...
Objective: To determine whether molecular karyotyping using multiple ligation probe amplification (M...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
Introduction: Turner syndrome is a genetic disorder in females and is the result of complete or part...
OBJECTIVE: To estimate whether multiplex ligation-dependent probe amplification (MLPA), a molecular ...
OBJECTIVE: To test whether multiplex ligation-dependent probe amplification (MLPA) can be used for t...
OBJECTIVE: To estimate whether multiplex ligation-dependent probe amplification (MLPA), a molecular ...
Average age at dianogsis,clinical features,and karyotype analysis of 40 girls with turner,s Syndrome...
Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More ...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
The past decade produced important advances in molecular genetic techniques potentially supplanting ...
Abstract Background Ultrasensitive assays to measure pre-pubertal gonadotropins levels could help id...
Abstract Background Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well...
AIMS: We aimed at evaluating a standard multiplex ligation-dependent probe amplification (MLPA) ...
Abstract Aims: We aimed at evaluating a standard multiplex ligation-dependent probe amplification (...
Turner syndrome (TS) is one of the most common chromosomal abnormalities among girls. Complete monos...
Objective: To determine whether molecular karyotyping using multiple ligation probe amplification (M...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
Introduction: Turner syndrome is a genetic disorder in females and is the result of complete or part...
OBJECTIVE: To estimate whether multiplex ligation-dependent probe amplification (MLPA), a molecular ...
OBJECTIVE: To test whether multiplex ligation-dependent probe amplification (MLPA) can be used for t...
OBJECTIVE: To estimate whether multiplex ligation-dependent probe amplification (MLPA), a molecular ...
Average age at dianogsis,clinical features,and karyotype analysis of 40 girls with turner,s Syndrome...
Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More ...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
The past decade produced important advances in molecular genetic techniques potentially supplanting ...
Abstract Background Ultrasensitive assays to measure pre-pubertal gonadotropins levels could help id...
Abstract Background Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well...