Turner syndrome (TS) is one of the most common chromosomal abnormalities, which is characterized by the partial or complete loss of one of the two X chromosomes. It is an important cause of short stature and ovarian failure in females. TS occurs in about one in every 1500-2500 live births
Turner syndrome is disease caused by monosomy or other abnormalities of chromosome X. This syndrome ...
Turner syndrome is a well-known cause of proportionately short stature in girls, but its frequency a...
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...
Turner syndrome (TS) affects approximately 1 out of every 1500–2500 live female births, with clinica...
Turner Syndrome is caused by absence of all or part of one copy of the X chromosome. Postnatally, th...
International audienceTurner syndrome (TS; ORPHA 881) is a rare condition in which all or part of on...
Turner syndrome (TS) is a common chromosomaldisorder. Turner syndrome (TS) also known as Ulrich–Tu...
Turner syndrome (TS) is a genetic anomaly occurring in women with worldwide frequency 1:2,000. Turne...
Turner’s Syndrome is a well recognized endocrine genetic disorder, characterized clinically by short...
Turner syndrome (TS) is a cross-cultural genetic disorder that affects around 1 in 2500 women and is...
Objective: Turner syndrome (TS) is one of the most common chromosomal abnormalities and an important...
Turner syndrome (TS), one of the most common sex chromosome disorders, is caused by numeric or struc...
Turner syndrome (TS) affects 1 in 2500 females. Monosomy X is the most common etiology, classically ...
Seven women in three generations of a family have been affected by Turner syndrome. Turner phenotype...
Turner syndrome is disease caused by monosomy or other abnormalities of chromosome X. This syndrome ...
Turner syndrome is a well-known cause of proportionately short stature in girls, but its frequency a...
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...
Turner syndrome (TS) affects approximately 1 out of every 1500–2500 live female births, with clinica...
Turner Syndrome is caused by absence of all or part of one copy of the X chromosome. Postnatally, th...
International audienceTurner syndrome (TS; ORPHA 881) is a rare condition in which all or part of on...
Turner syndrome (TS) is a common chromosomaldisorder. Turner syndrome (TS) also known as Ulrich–Tu...
Turner syndrome (TS) is a genetic anomaly occurring in women with worldwide frequency 1:2,000. Turne...
Turner’s Syndrome is a well recognized endocrine genetic disorder, characterized clinically by short...
Turner syndrome (TS) is a cross-cultural genetic disorder that affects around 1 in 2500 women and is...
Objective: Turner syndrome (TS) is one of the most common chromosomal abnormalities and an important...
Turner syndrome (TS), one of the most common sex chromosome disorders, is caused by numeric or struc...
Turner syndrome (TS) affects 1 in 2500 females. Monosomy X is the most common etiology, classically ...
Seven women in three generations of a family have been affected by Turner syndrome. Turner phenotype...
Turner syndrome is disease caused by monosomy or other abnormalities of chromosome X. This syndrome ...
Turner syndrome is a well-known cause of proportionately short stature in girls, but its frequency a...
Forty five cases of Turner syndrome diag-nosed in the Genetics Clinic, between January 1986 and Dece...
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