Disease: Chromosome 16- trisomy 16q
- A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature
- Absence of Prenatal Forebrain Defects in the Dp(16)1Yey/+ Mouse Model of Down Syndrome
- Bilateral anterior segment dysgenesis in an infant with partial trisomy 16q and partial monosomy 3p
- Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement
- Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication
- Clinical, cytogenetic and molecular-cytogenetic characterization of a patient with a de novo tandem proximal-intermediate duplication of 16q and review of the literature
- Diagnosis of a fetus with a de novo 16q partial trisomy syndrome
- Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature
- Mechanisms of formation of structural variation in a fully sequenced human genome
- Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
- Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report
- Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature
- Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)
- Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
- Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: molecular characterization of two der(11)t(11;16)
- The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese population
- The first case of a patient with de novo partial distal 16q tetrasomy and a data's review
- Ts1Cje Down syndrome model mice exhibit environmental stimuli-triggered locomotor hyperactivity and sociability concurrent with increased flux through central dopamine and serotonin metabolism