✦ LIBER ✦

A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome

✍ Scribed by Tae Sung Park; Sang-Guk Lee; Jaewoo Song; Jin Seok Kim; Jong Rak Choi

Publisher: Springer
Year: 2009
Tongue: English
Weight: 170 KB
Volume: 89
Category: Article
ISSN: 0939-5555
DOI: 10.1007/s00277-009-0814-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Myelodysplastic syndrome in a child with

Myelodysplastic syndrome in a child with 15q24 deletion syndrome

✍ Yoko Narumi; Masaaki Shiohara; Keiko Wakui; Asahito Hama; Seiji Kojima; Kentaro 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 242 KB 👁 1 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

A case of myelodysplastic syndrome with

A case of myelodysplastic syndrome with erythroid hypoplasia associated with a familial translocation t(3;14)(p21.1;q24.1)

✍ Günçağ Dinçol; Şükrü Öztürk; Şükrü Palanduz; Gülçin Tutkan; Naciye Yıldırım; Mes 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB 👁 3 views

Long-term survival in a patient with del

Long-term survival in a patient with del(18)(q12.2q21.1)

✍ Tinkle, Brad T. ;Christianson, Carol A. ;Schorry, Elizabeth K. ;Webb, Thomas ;Ho 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 1 views

## Abstract The 18q‐ syndrome is relatively common among cytogenetic abnormalities occurring in approximately 1 in 40,000 live births. However, interstitial deletions involving 18q12.2 to q21.1 are much less common. Only 15 cases have been reported in the literature. A phenotypic pattern is emergin

Constitutional translocation t(1;17)(p36

Constitutional translocation t(1;17)(p36;q12–21) in a patient with neuroblastoma

✍ Dr. Geneviève Laureys; Frank Speleman; Ghislain Opdenakker; Yves Benoit; Jules L 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 307 KB 👁 1 views

## Abstract A constitutional chromosome translocation t(1;17)(p36;q12–21) is reported in a boy with neuroblastoma. This is the first description of a cytogenetic abnormality possibly predisposing to the development of neuroblastoma.

A novel gene, MDS2, is fused to ETV6/TEL

A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome

✍ María D. Odero; José L. Vizmanos; José P. Román; Idoya Lahortiga; Carlos Panizo; 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 658 KB

## Abstract __ETV6/TEL__ is the first transcription factor identified that is specifically required for hematopoiesis within the bone marrow. This gene has been found to have multiple fusion partners of which 16 have been cloned. Fluorescence in situ hybridization (FISH) analysis in a patient with