Down Syndrome (DS), trisomy 21, is the most common chromosomal syndrome that affects one in 600-800 live births. The advanced maternal age is the only well known risk factor to cause DS. Our study revealed that many young mothers produced DS children than advanced age mothers in India. A total of 150 suspected DS cases were investigated cytogenetically. Randomly selected 200 healthy families in South India were used as controls. Logistic regression was performed on case-control dataset which was generated by randomly selecting the child from each of the control families. Pedigree analyses indicated that the maternal grandmothers had advanced age during conception of their daughters who gave birth to DS child. Case-control status was used as...
Studies were conducted in 222 children clinically diagnosed with Down syndrome (properly diagnosed o...
Background and Objective: Down syndrome is a genetic disorder due to trisomy of 21 chromosome, which...
Down syndrome (DS) originates, in most of the cases (95 %), from a full trisomy of chromosome 21. Th...
Down Syndrome (DS), trisomy 21, is the most common chromosomal syndrome that affects one in 600-800 ...
Abstract Background Down syndrome (DS) is the most common chromosomal anomaly associated with mental...
Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This i...
Background: Down Syndrome (DS) is the most common chromosomal anomaly associated with mental retarda...
Chromosomal syndromes contribute significantly to reproductive failure, birth defects, mental retard...
ABSTRACT Majority of the chromosomal abnormalities are incompatible with embryonic or fetal survival...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
Down syndrome (DS) is the most common live-born birth defect in humans. The genetic cause of DS is t...
AbstractDown syndrome is a common chromosomal anomaly causing multiple congenital malformations and ...
Introduction: Down Syndrome is a common chromosome abnormality among infants. This condition is Pres...
Purpose: Children born to older parents are at greater risk for genetic abnormalities, such as Down ...
Studies were conducted in 222 children clinically diagnosed with Down syndrome (properly diagnosed o...
Background and Objective: Down syndrome is a genetic disorder due to trisomy of 21 chromosome, which...
Down syndrome (DS) originates, in most of the cases (95 %), from a full trisomy of chromosome 21. Th...
Down Syndrome (DS), trisomy 21, is the most common chromosomal syndrome that affects one in 600-800 ...
Abstract Background Down syndrome (DS) is the most common chromosomal anomaly associated with mental...
Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This i...
Background: Down Syndrome (DS) is the most common chromosomal anomaly associated with mental retarda...
Chromosomal syndromes contribute significantly to reproductive failure, birth defects, mental retard...
ABSTRACT Majority of the chromosomal abnormalities are incompatible with embryonic or fetal survival...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
Down syndrome (DS) is the most common live-born birth defect in humans. The genetic cause of DS is t...
AbstractDown syndrome is a common chromosomal anomaly causing multiple congenital malformations and ...
Introduction: Down Syndrome is a common chromosome abnormality among infants. This condition is Pres...
Purpose: Children born to older parents are at greater risk for genetic abnormalities, such as Down ...
Studies were conducted in 222 children clinically diagnosed with Down syndrome (properly diagnosed o...
Background and Objective: Down syndrome is a genetic disorder due to trisomy of 21 chromosome, which...
Down syndrome (DS) originates, in most of the cases (95 %), from a full trisomy of chromosome 21. Th...