Assistente RarasDescreva sintomas, busque uma doença ou conte sua história. Eu pesquiso em 10.468 doenças raras.
Raras pode cometer erros. Não substitui orientação médica profissional.
Nenhum ensaio clínico registrado para esta condição.
Clinical and Molecular Presentation of a Patient with Paternal Uniparental Isodisomy of Chromosome 16.
Endocrine Abnormalities in Mosaic Trisomy 16 Adolescent: A Case Report.
Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results.
Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterine growth restriction, intrauterine fetal death, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line.
Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array.