✦ LIBER ✦

Translocation(Y;1)(q12;q12) in hematologic malignancies: Report on Two New Cases, FISH Characterization, and Review of the Literature

✍ Scribed by Lucienne Michaux; Iwona Wlodarska; Elvira Rodrigues Pereira Velloso; Gregor Verhoef; Angeline Van Orshoven; Jean-Louis Michaux; Jean-Marie Scheiff; Cristina Mecucci; Herman Van den Berghe

Book ID: 113253599
Publisher: Elsevier Science
Year: 1996
Tongue: English
Weight: 338 KB
Volume: 86
Category: Article
ISSN: 0165-4608
DOI: 10.1016/0165-4608(95)00141-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

8q12.1q12.3 de novo microdeletion involv

8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: Case report and critical review of the literature

✍ Orazio Palumbo; Pietro Palumbo; Raffaella Stallone; Teresa Palladino; Leopoldo Z 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 664 KB

Jumping Translocations Involving Chromos

Jumping Translocations Involving Chromosome 1q in a Patient with Crohn Disease and Acute Monocytic Leukemia: A Review of the Literature on Jumping Translocations in Hematological Malignancies and Crohn Disease

✍ K.S Reddy; L Parsons; L Colman 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 243 KB

Cytogenetic abnormalities in hepatoblast

Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12

✍ Toshihito Nagata; Masanori Nakamura; Hiroyuki Shichino; Motoaki Chin; Kiminobu S 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 231 KB

Common features of myeloproliferative di

Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110–FGFR1 fusion: Report of a new case and review of the literature

✍ Marie-Joëlle Mozziconacci; Nadine Carbuccia; Thomas Prebet; Aude Charbonnier; An 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 98 KB

Microdeletion del(22)(q12.2) encompassin

Microdeletion del(22)(q12.2) encompassing the facial development-associated gene,MN1(meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature

✍ Tom B Davidson, Pedro A Sanchez-Lara, Linda M Randolph, Mark D Krieger, Shi-Qi W 📂 Article 📅 2012 🏛 BioMed Central 🌐 English ⚖ 470 KB