Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Joann Meekins"'
Publikováno v:
Leukemia. 21:842-844
A novel NUP98-PHF23 fusion resulting from a cryptic translocation t(11;17)(p15;p13) in acute myeloid leukemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5235b229b697f425e12ad73d1ec976
https://doi.org/10.1038/sj.leu.2404579
https://doi.org/10.1038/sj.leu.2404579
Autor:
Michael J. Ronnenburg, Yi Ning, Melody Butler, Candice N. Ament, Jessica A. Crowley, Joann Meekins
Publikováno v:
Cancer genetics and cytogenetics. 157(1)
Deletions in the long arm of chromosome 6 are one of the most commonly observed chromosome aberrations in lymphoid malignancies and have been identified as an adverse prognostic factor in subsets of leukemia and lymphoma. Although large deletions can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7e6b5c13052033906bbcf47f9a04d0
https://pubmed.ncbi.nlm.nih.gov/15676153
https://pubmed.ncbi.nlm.nih.gov/15676153
Publikováno v:
American Journal of Medical Genetics Part A. :2906-2907
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f6893857966de3dc0ea1da45d8af44f
https://doi.org/10.1002/ajmg.a.33691
https://doi.org/10.1002/ajmg.a.33691
Publikováno v:
Cancer Genetics and Cytogenetics. 19:291-299
Chromosomal abnormalities were demonstrated in the bone marrow cultures of two patients with acquired idiopathic sideroblastic anemia (AISA). Both patients subsequently experienced leukemic transformation and developed acute myelomonocytic leukemia (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16cdab93b66276db23a01237ceac0452
https://doi.org/10.1016/0165-4608(86)90058-0
https://doi.org/10.1016/0165-4608(86)90058-0
Autor:
Chen-Chih J. Sun, Maimon M. Cohen, Stuart Schwartz, Joann Meekins, S. R. Panny, John M. Opitz
Publikováno v:
American Journal of Medical Genetics. 15:141-144
Cytogenetic study of a day-old infant showed a terminal del(7q): 46,XX,del(7)(pter leads to q32:). This infant had cebocephaly with holoprosencephaly. These clinical findings are atypical for the 7q - syndrome, in which patients usually have growth a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7477d3bddea05c9ddd6566e6a36058f3
https://doi.org/10.1002/ajmg.1320150119
https://doi.org/10.1002/ajmg.1320150119
Publikováno v:
Cancer genetics and cytogenetics. 10(2)
A consistent chromosomal abnormality t(6;9)(p23;q34) was demonstrated in the bone marrow or unstimulated peripheral blood cultures of two patients with acute nonlymphocytic leukemia (ANLL). Only two additional cases with ANLL and a similar cytogeneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80f674b588576a4a63aa37482c45cce9
https://pubmed.ncbi.nlm.nih.gov/6616433
https://pubmed.ncbi.nlm.nih.gov/6616433