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Page 1
Karyotype evolution in a patient with biphenotypic neonatal leukemia.
Fugazza G, Basso G, Sessarego M, Haupt R, Comelli A, Roncella S, Negri D, Sansone R. Fugazza G, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1992 Sep;62(2):124-9. doi: 10.1016/0165-4608(92)90249-8. Cancer Genet Cytogenet. 1992. PMID: 1394096
Pentasomy 21 in leukemia complicating Diamond-Blackfan anemia.
Mori PG, Haupt R, Fugazza G, Sessarego M, Corcione A, Strigini P, Sansone R. Mori PG, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1992 Oct 1;63(1):70-2. doi: 10.1016/0165-4608(92)90067-i. Cancer Genet Cytogenet. 1992. PMID: 1423230
ins(6;1) in a patient with congenital leukemia.
Sansone R, Sessarego M, Haupt R, Garré ML, Strigini P. Sansone R, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1989 Jan;37(1):19-22. doi: 10.1016/0165-4608(89)90069-1. Cancer Genet Cytogenet. 1989. PMID: 2917330
Carcinoid syndrome.
Granata C, Haupt R, Mazzaferro V, Fratino G, Mattioli G, Gasparini M, De Bernardi B. Granata C, et al. Among authors: haupt r. Pediatr Surg Int. 1996 Jun;11(5-6):398-9. doi: 10.1007/BF00497825. Epub 2013 Sep 21. Pediatr Surg Int. 1996. PMID: 24057728
429 results