Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eva Perdahl-Wallace"'
Publikováno v:
Pediatric Blood & Cancer. 65:e27267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dca69a6838fd99e1a5996094c3cc697
https://doi.org/10.1002/pbc.27267
https://doi.org/10.1002/pbc.27267
Autor:
Syed Zaman, Jay Greenberg, Bridget Smith, JoAnna Zgoda, Eva Perdahl-Wallace, Aurelia Meloni-Ehrig, Philip N. Mowrey
Publikováno v:
Cancer Genetics and Cytogenetics. 191:43-45
We report a case of congenital embryonal rhabdomyosarcoma (ERMS), a rare form of rhabdomyosarcoma, featuring a karyotype with a t(2;8)(q35;q13) in a 2-week-old male infant. This is the third reported case of congenital ERMS with cytogenetic findings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c229966a0daf9cc6037575d02af777
https://doi.org/10.1016/j.cancergencyto.2009.01.010
https://doi.org/10.1016/j.cancergencyto.2009.01.010
Publikováno v:
Clinical Pediatrics. 45:187-189
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d3df8aab95b10a7ba59f0fefaf32540
https://doi.org/10.1177/000992280604500212
https://doi.org/10.1177/000992280604500212
Autor:
Eva Perdahl-Wallace, Vesna Najfeld, Chris Theodossiou, Lewis B. Silverman, Angela Scalise, Kevin Troy
Publikováno v:
Cancer Genetics and Cytogenetics. 63:89-94
We report three patients with acute lymphoblastic leukemia with biphenotypic and early progenitor phenotype who had del(5q). In the first patient, the del(5q) was the sole abnormality; in the second patient, the del(5q) was interpreted as subclonal e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76aa46b689ed16bc184a062820edb0b3
https://doi.org/10.1016/0165-4608(92)90385-l
https://doi.org/10.1016/0165-4608(92)90385-l