Nonsyndromic total anomalous venous return associated with a de novo translocation inolving chromosomes 10 and 21 t(10;21)(q23.1;q11.2)
Francesco Acquati(University of Insubria), Maurizio Papa(IRCCS Ospedale San Raffaele), Monica Taborelli(Institute of Oncology Research), Antonella Russo, Maria Grazia Tibiletti(University of Insubria), Chiara Camesasca(IRCCS Ospedale San Raffaele), Roberto Taramelli(University of Insubria)
American Journal of Medical Genetics
January 1, 2000
Cited by 9
Related Papers
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
|Genetics in Medicine|2019|666
Genomic and expression profiling identifies the B‐cell associated tyrosine kinase Syk as a possible therapeutic target in mantle cell lymphoma
|British Journal of Haematology|2005|193
Genome-wide DNA profiling of marginal zone lymphomas identifies subtype-specific lesions with an impact on the clinical outcome
|Blood|2010|189
Inheritance in idiopathic premature ovarian failure: analysis of 71 cases
|Human Reproduction|1998|166
Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study
|Digestive and Liver Disease|2013|158