✦ LIBER ✦

A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat

✍ Scribed by Imke Veltman; Martien van Asseldonk; Marga Schepens; Hans Stoop; Leendert Looijenga; Cokkie Wouters; Lutgarde Govaerts; Ron Suijkerbuijk; Ad Geurts van Kessel

Book ID: 114135321
Publisher: Elsevier Science
Year: 2002
Tongue: English
Weight: 518 KB
Volume: 136
Category: Article
ISSN: 0165-4608
DOI: 10.1016/s0165-4608(01)00666-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A complex translocation, t(4;11;13)(q21;

A complex translocation, t(4;11;13)(q21;q23;q12–14), in a case of infantile acute lymphoblastic leukemia

✍ Alison T. Matsunaga; Habib Torfi; James Feusner 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 213 KB

A case of Prader – Willi syndrome arisin

A case of Prader – Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13)

✍ Malgorzata Krajewska Walasek; Anna Gutkowska; Beata Bielińska; Bozenna Goryluk-K 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 996 KB

De novo AML with trilineage myelodysplas

De novo AML with trilineage myelodysplasia and a novel t(11;12)(p15;q13)

✍ K.F Wong; Y.L Kwong; C.C So 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 190 KB

Molecular analysis of a familial case of

Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

✍ Marc J. Eleveld; Daniëlle Bodmer; Gerard Merkx; Angélique Siepman; Sandra H. E. 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 233 KB

## Abstract We identified a novel familial case of clear‐cell renal cancer and a t(3;6)(q12;q15). Subsequent cytogenetic and molecular analyses showed the presence of several abnormalities within tumour samples obtained from different patients. Loss of the der(3) chromosome was noted in some, but n

Primary cutaneous follicle center lympho

Primary cutaneous follicle center lymphoma of the arm with a novel chromosomal translocation t(12;21)(q13;q22): A case report

✍ Tomislav M. Jelic; Paula K. Berry; Steven J. Jubelirer; Lisa Plumley; Paul H. Ha 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 367 KB 👁 2 views

A case of atypical myelodysplastic syndr

A case of atypical myelodysplastic syndrome with micromegakaryocytes, normal platelet count, and t(3;12)(q21;p13) with inv(3)(q21q26)

✍ Susanne Schnittger; Claudia Schoch; Berthold Streubel; Hans-Fokke Hinrichs; Burk 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 702 KB

A 49-year-old woman patient with atypical myelodysplastic syndrome (MDS) showing a der(3)t(3;12)(q21;p13), and der(12)t(3; 12)(q21;p13)inv(3)(q21q26) as an acquired chromosomal abnormality in the bone marrow is described. The chromosomal breakpoints of the presented complex aberration with combinati