✦ LIBER ✦

Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

✍ Scribed by Sibel Oguzkan; Yunus Kasım Terzi; Elif Güler; Murat Derbent; Pınar Isık Agras; Umit Saatci; Sukriye Ayter

Book ID: 113512801
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 166 KB
Volume: 164
Category: Article
ISSN: 0165-4608
DOI: 10.1016/j.cancergencyto.2005.08.004

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Two novel mutations of the NF1 gene in C

Two novel mutations of the NF1 gene in Chinese Han families with type 1 neurofibromatosis

✍ Cai, Yejun; Fan, Zhipeng; Liu, Qingjie; Li, Jingyuan; Du, Juan; Shen, Yan; Wang, 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 161 KB

Identification of two novel mutations in

Identification of two novel mutations in the NF1 gene in Chinese patients with neurofibromatosis type 1

✍ Bin Chen; Liang-Dan Sun; Fu-Sheng Zhou; Feng-Ming Yao; Cheng Quan; Qiao-Yun Fang 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 799 KB

A Clinical Variant of Neurofibromatosis

A Clinical Variant of Neurofibromatosis Type 1: Familial Spinal Neurofibromatosis with a Frameshift Mutation in the NF1 Gene

✍ Elisabet Ars; Helena Kruyer; Antonia Gaona; Pilar Casquero; Jordi Rosell; Víctor 📂 Article 📅 1998 🏛 American Society of Human Genetics 🌐 English ⚖ 310 KB

NF1 gene analysis focused on CpG-rich ex

NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1

✍ E. Girodon Boulandet; J. Pantel; C. Cazeneuve; M. Van Gijn; D. Vidaud; S. Lemay; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB 👁 2 views

Gross deletions of the neurofibromatosis

Gross deletions of the neurofibromatosis type 1(NF1)gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay

✍ M. Upadhyaya; M. Ruggieri; J. Maynard; M. Osborn; C. Hartog; S. Mudd; M. Penttin 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 119 KB

Toward a Survey of Somatic Mutation of t

Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1

✍ Ingrid Eisenbarth; Kim Beyer; Winfrid Krone; Günter Assum 📂 Article 📅 2000 🏛 American Society of Human Genetics 🌐 English ⚖ 199 KB