Turner Syndrome occurs in one out of every 5000 live female births and the diagnosis is usually based on the clinical presentation. In the last 9 years, 17 of 1681 patients who underwent cytogenetic evaluation to investigate uncertain chromosomal anomaly had Turner syndrome. Ten of the patients were the 45,X (classic) type, 2 patients were 46,X,i(Xq), 1 patient was 46,X,der(X)del(X)(p22.1) del(X)(q26), and 4 were mosaic (2 were 45,X/46,XY and the other 2 were 45,X/47,XXX). Detailed clinical evaluations of these patients are presented. © 2012 by The American Society for Clinical Pathology
Turner syndrome, characterized by monosomy of X chromosome, has a peculiar phenotype, including shor...
Of 130, mostly prepubertal girls with features of Turner's syndrome, 89 had an abnormal sex chromoso...
The aim of this study is to evaluate the link of chromosome constitution in Turner syndrome and in d...
Forty five cases of Turner syndrome diag-nosed in the Genetics Clinic, between January 1986 and Dece...
Turner syndrome (TS) is a genetic disorder which is characterized by the complete or partial absence...
BACKGROUND: Turner's syndrome (TS) is a sex chromosome disorder occurring in I in 2,500 female birth...
Turner syndrome (TS) affects 1 in 2500 females. Monosomy X is the most common etiology, classically ...
ABSTRACT: BACKGROUND: Small supernumerary marker chromosomes (sSMC) can be present in numerically ab...
Although Turner syndrome is most commonly associated with a 45,X genotype, other mosaic genotypes ar...
Turner syndrome (TS) is a common chromosomaldisorder. Turner syndrome (TS) also known as Ulrich–Tu...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
Turner syndrome (TS) is a common genetic disorder in females associated with the absence of complete...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
WOS: 000441304600021Objective: Turner syndrome (TS) is the result of partial or complete loss of the...
Turner Syndrome is characterized by a normal X chromosome and the partial or complete absence of a s...
Turner syndrome, characterized by monosomy of X chromosome, has a peculiar phenotype, including shor...
Of 130, mostly prepubertal girls with features of Turner's syndrome, 89 had an abnormal sex chromoso...
The aim of this study is to evaluate the link of chromosome constitution in Turner syndrome and in d...
Forty five cases of Turner syndrome diag-nosed in the Genetics Clinic, between January 1986 and Dece...
Turner syndrome (TS) is a genetic disorder which is characterized by the complete or partial absence...
BACKGROUND: Turner's syndrome (TS) is a sex chromosome disorder occurring in I in 2,500 female birth...
Turner syndrome (TS) affects 1 in 2500 females. Monosomy X is the most common etiology, classically ...
ABSTRACT: BACKGROUND: Small supernumerary marker chromosomes (sSMC) can be present in numerically ab...
Although Turner syndrome is most commonly associated with a 45,X genotype, other mosaic genotypes ar...
Turner syndrome (TS) is a common chromosomaldisorder. Turner syndrome (TS) also known as Ulrich–Tu...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
Turner syndrome (TS) is a common genetic disorder in females associated with the absence of complete...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
WOS: 000441304600021Objective: Turner syndrome (TS) is the result of partial or complete loss of the...
Turner Syndrome is characterized by a normal X chromosome and the partial or complete absence of a s...
Turner syndrome, characterized by monosomy of X chromosome, has a peculiar phenotype, including shor...
Of 130, mostly prepubertal girls with features of Turner's syndrome, 89 had an abnormal sex chromoso...
The aim of this study is to evaluate the link of chromosome constitution in Turner syndrome and in d...