Andere Kunden interessierten sich auch für
![Rett Syndrome mutations: molecular alterations at neuronal synapses]( "Rett Syndrome mutations: molecular alterations at neuronal synapses")
Rett Syndrome mutations: molecular alterations at neuronal synapses32,99 €![Relation of some gene polymorphisms with metabolic syndrome in women]( "Relation of some gene polymorphisms with metabolic syndrome in women")
Relation of some gene polymorphisms with metabolic syndrome in women27,99 €![Hormonal key players for obesity in Children with Down Syndrome]( "Hormonal key players for obesity in Children with Down Syndrome")
Hormonal key players for obesity in Children with Down Syndrome46,99 €![Molecular Diagnosis of Intellectual Disability]( "Molecular Diagnosis of Intellectual Disability")
Molecular Diagnosis of Intellectual Disability26,99 €![Modification of Ti Plasmid to Construction dTi Vector for Gene Cloning]( "Modification of Ti Plasmid to Construction dTi Vector for Gene Cloning")
Modification of Ti Plasmid to Construction dTi Vector for Gene Cloning32,99 €![Cloning of oil degradation genes]( "Cloning of oil degradation genes")
Cloning of oil degradation genes44,99 €![Mycoplasma Recombinant vaccine]( "Mycoplasma Recombinant vaccine")
Mycoplasma Recombinant vaccine26,99 €
Birth defects occur in ~4-5% of all live births, and are second only to accidents as the most common cause of death in children. These congenital anomalies consist of both functional/metabolic and structural defects including those affecting the central nervous system, heart, urogenital system, and craniofacial development. Genetic causes are important in these developmental disorders, but the molecular basis for most congenital anomalies is not known. The elucidation of genetic etiologies of congenital anomalies is hampered by the lack of realistic candidate genes to study. Those rare, but extremely valuable and underutilized patients with a developmental disorder that harbor "balanced" chromosomal rearrangements provide a unique opportunity to identify new causative genes important in human development. Results from this genetic research will lead to the identification of new genes with important functions in human development and the genesis of congenital anomalies. The use ofpositional cloning techniques in patients with developmental disorders who have balanced chromosomal rearrangements will enable the detection of novel, etiologic genes.