✦ LIBER ✦

Deep intronic mutations are rarely a cause of hemophilia B

✍ Scribed by Jinong Feng; Qiang Liu; Joni Drost; Steve S. Sommer

Publisher: John Wiley and Sons
Year: 1999
Tongue: English
Weight: 89 KB
Volume: 14
Category: Article
ISSN: 1059-7794
DOI: 10.1002/(sici)1098-1004(1999)14:3<267::aid-humu11>3.0.co;2-i

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

NTNG1 mutations are a rare cause of Rett

NTNG1 mutations are a rare cause of Rett syndrome

✍ Hayley L. Archer; Julie C. Evans; David S. Millar; Peter W. Thompson; Alison M. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB 👁 1 views

Mutations in TPM3 are a common cause of

Mutations in TPM3 are a common cause of congenital fiber type disproportion

✍ Nigel F. Clarke; Hanna Kolski; Danielle E. Dye; Esther Lim; Robert L. L. Smith; 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB

CHMP2B mutations are not a cause of deme

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia

✍ Patrizia Rizzu; Saskia E. van Mil; Burcu Anar; Sonia M. Rosso; Laura Donker Kaat 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 51 KB 👁 2 views

Magnetic resonance imaging-detected lymp

Magnetic resonance imaging-detected lymph nodes close to the mesorectal fascia are rarely a cause of margin involvement after total mesorectal excision

✍ O. C. Shihab; P. Quirke; R. J. Heald; B. J. Moran; G. Brown 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 176 KB 👁 1 views

A one-step DGGE scanning method for dete

A one-step DGGE scanning method for detection of mutations in the K-, N-, and H-ras oncogenes: Mutations at codons 12, 13 and 61 are rare in B-cell non-Hodgkin's lymphoma

✍ Trine Nedergaard; Per Guldberg; Elisabeth Ralfkiaer; Jesper Zeuthen 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 French ⚖ 113 KB 👁 2 views

Mutations in the N-, K-, and H-ras genes are key events in the process of carcinogenesis of many human cancers and may serve as important targets for therapeutic intervention. We developed a simple diagnostic method that in one step and within 5 hr determines the mutational status of any of the 3 ra

A single nucleotide polymorphism in the

A single nucleotide polymorphism in the 3′untranslated region of the CDKN2A gene is common in sporadic primary melanomas but mutations in the CDKN2B, CDKN2C, CDK4 and p53 genes are rare

✍ Rajiv Kumar; Johanna Smeds; Petra Berggren; Oddbjørn Straume; Barbro Lundh Rozel 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 French ⚖ 142 KB 👁 2 views