• "De novo" partial trisomy 16p (author's transl)
• "Molecular rulers" for calibrating phenotypic effects of telomere imbalance
• A case of insertional translocation resulting in partial trisomy 16p
• Abnormality of chromosome 16 and its phenotypic expression
• Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D1
• Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation
• Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)
• Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis
• De novo trisomy 16p
• Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities
• Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation
• Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature
• Familial transmission of 16p trisomy in an infant
• Long-term follow-up of a 26-year-old male with duplication of 16p: clinical report and review
• Myelodysplastic syndrome in a kindred with ins(16) (p11.2)
• Myelodysplastic syndrome with an unbalanced 1;16 translocation in a case of early age of onset
• No evidence of partial trisomy 16p in an autistic calendar savant with Tourette syndrome
• Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report
• Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
• Partial trisomy 16p (16p12.2pter) and partial monosomy 22q (22q13.31 qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
• Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome
• Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter)
• Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester
• Prenatal diagnosis of partial trisomy 16p and its association with congenital diaphragmatic hernia
• Pulmonary hypertension and trisomy 16
• Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter
• Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13)
• Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16
• Trisomy 16p in a liveborn infant and review of trisomy 16p
• Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature
• Trisomy 16p: a longitudinal profile and photo essay
• Trisomy 16q21 = to qter
• Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy
• Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13
• Two unbalanced segregation products due to a maternal t(7;16)inv(16)
• Unbalanced 5;16 translocation in a boy with papillary thyroid carcinoma
• Value of chromosome painting in determining the chromosomal outcome in offspring of a 12;16 translocation carrier
• Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer
• X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation