Background: Down Syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This is due to the occurrence of free trisomy 21 (92–95 %), mosaic trisomy 21 (2–4 %) and translocation (3–4 %). Advanced maternal age is a well documented risk factor for maternal meiotic nondisjunction. In India three children with DS are born every hour and more DS children are given birth to by young age mothers than by advanced age mothers. Therefore, detailed analysis of the families with DS is needed to find out other possible causative factors for nondisjunction. Methods: We investigated 69 families of cytogenetically confirmed DS children and constructed pedigrees of these families. We also studied 200 randomly selected familie...
The Centers for Disease Control and Prevention (CDC) estimates that about 6,000 babies are born with...
Introduction: We investigated the possible maternal risk factors that mayincrease the incidence of D...
Objective: Down syndrome is a common genetic disease, diagnosed with congenital malformation/mental ...
Background: Down Syndrome (DS) is the most common chromosomal anomaly associated with mental retarda...
Abstract Background Down syndrome (DS) is the most common chromosomal anomaly associated with mental...
Down syndrome (DS), trisomy 21, is the most common chromosomal syndrome that affects one in 600-800 ...
Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This i...
Down syndrome (DS) is the most common live-born birth defect in humans. The genetic cause of DS is t...
Down syndrome (DS) originates, in most of the cases (95 %), from a full trisomy of chromosome 21. Th...
Down syndrome is a common chromosomal anomaly causing multiple congenital malformations and mental r...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
AbstractDown syndrome is a common chromosomal anomaly causing multiple congenital malformations and ...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
ABSTRACT Majority of the chromosomal abnormalities are incompatible with embryonic or fetal survival...
Trisomy 21 (Down Syndrome) is the model human phenotype for all genome gain-dosage imbalance situati...
The Centers for Disease Control and Prevention (CDC) estimates that about 6,000 babies are born with...
Introduction: We investigated the possible maternal risk factors that mayincrease the incidence of D...
Objective: Down syndrome is a common genetic disease, diagnosed with congenital malformation/mental ...
Background: Down Syndrome (DS) is the most common chromosomal anomaly associated with mental retarda...
Abstract Background Down syndrome (DS) is the most common chromosomal anomaly associated with mental...
Down syndrome (DS), trisomy 21, is the most common chromosomal syndrome that affects one in 600-800 ...
Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This i...
Down syndrome (DS) is the most common live-born birth defect in humans. The genetic cause of DS is t...
Down syndrome (DS) originates, in most of the cases (95 %), from a full trisomy of chromosome 21. Th...
Down syndrome is a common chromosomal anomaly causing multiple congenital malformations and mental r...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
AbstractDown syndrome is a common chromosomal anomaly causing multiple congenital malformations and ...
Background: Down syndrome (DS) and sex chromosomal aneuploidy (SA) are common chromosomal anomalies ...
ABSTRACT Majority of the chromosomal abnormalities are incompatible with embryonic or fetal survival...
Trisomy 21 (Down Syndrome) is the model human phenotype for all genome gain-dosage imbalance situati...
The Centers for Disease Control and Prevention (CDC) estimates that about 6,000 babies are born with...
Introduction: We investigated the possible maternal risk factors that mayincrease the incidence of D...
Objective: Down syndrome is a common genetic disease, diagnosed with congenital malformation/mental ...