Trisomy 9p resulting from maternal 9/21 translocation
Related Experiment Videos
Human Genetics
|May 19, 1976
Abstract:
The clinical picture found in a child with trisomy 9p confirmed that this chromosomal syndrome is a entity, which arises from maternal translocation t(9;21).
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencing.
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti·2026
The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti·2024
The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024).
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti·2024
The association of factor V Leiden with various clinical patterns of venous thromboembolism-the factor V Leiden paradox.
QJM : monthly journal of the Association of Physicians·2014
Positive Urine Cultures for Enterococcus spp. vs. Escherichia coli in Febrile Infants Younger Than 90 Days: A Matched Cohort Study.
Acta paediatrica (Oslo, Norway : 1992)·2026
Lenticulostriate vasculopathy in neonates: An imaging marker with heterogeneous clinical significance.
Radiology case reports·2026
Novel ABCC2 mutations in a neonate with Dubin-Johnson syndrome: a case report.
Frontiers in endocrinology·2026
Caveolin-1-Mediated Tight Junction Assembly and Intestinal Permeability in Necrotizing Enterocolitis.
American journal of physiology. Gastrointestinal and liver physiology·2026