✦ LIBER ✦

Correction: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome

✍ Scribed by Hodgson, G.; Hager, J.H.; Volik, S.; Hariono, S.; Wernick, M.; Moore, D.; Nowak, N.; Albertson, D.G.; Pinkel, D.; Collins, C.; Hanahan, D.; Gray, J.W.

Book ID: 109918681
Publisher: Nature Publishing Group
Year: 2001
Tongue: English
Weight: 45 KB
Volume: 29
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1201-491c

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Erratum: Mutations in PTPN11, encoding t

Erratum: Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 95 KB

Electrocardiography in Noonan syndrome P

Electrocardiography in Noonan syndrome PTPN11 gene mutation—phenotype characterization

✍ Ellen A. Croonen; Ineke van der Burgt; Livia Kapusta; Jos M. Th. Draaisma 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 3 views

Mutational Analysis of PTPN11 Gene in Ta

Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome

✍ Chia-Sui Hung; Ju-Li Lin; Yann-Jinn Lee; Shuan-Pei Lin; Mei-Chyn Chao; Fu-Sung L 📂 Article 📅 2007 🏛 Chinese Electronic Periodical Services 🌐 English ⚖ 126 KB

Mutational analysis of the PTPN11 gene i

Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndrome

✍ Essawi, Mona L.; Ismail, Manal F.; Afifi, Hanan H.; Kobesiy, Maha M.; El Kotoury 📂 Article 📅 2013 🏛 Chinese Electronic Periodical Services 🌐 English ⚖ 704 KB

Clinical and hematologic findings in Noo

Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutations

✍ Murat Derbent; Yekta Oncel; Kürşad Tokel; Birgül Varan; Ayşegül Haberal; A. Cana 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 2 views

## Abstract Reports on Noonan syndrome (NS) have documented multiple types of coagulation defects and bleeding diathesis, and a wide range of clinical presentations. Early studies suggested that a large proportion of NS patients have coagulation defects, whereas more recent reports indicate low rat

No mutation in the gene for Noonan syndr

No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome

✍ Birte Tröger; Kerstin Kutsche; Hanno Bolz; Sabine Lüttgen; Andreas Gal; Zsuzsann 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 42 KB 👁 2 views