✦ LIBER ✦

Causal coding of stationary sources and individual sequences with high resolution

✍ Scribed by Linder, T.; Zamir, R.

Book ID: 114639066
Publisher: IEEE
Year: 2006
Tongue: English
Weight: 475 KB
Volume: 52
Category: Article
ISSN: 0018-9448
DOI: 10.1109/tit.2005.862075

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Joint Universal Lossy Coding and Identif

Joint Universal Lossy Coding and Identification of Stationary Mixing Sources With General Alphabets

✍ Raginsky, M. 📂 Article 📅 2009 🏛 IEEE 🌐 English ⚖ 398 KB

High-Resolution Multiple Wideband and No

High-Resolution Multiple Wideband and Nonstationary Source Localization With Unknown Number of Sources

✍ Wen-Jun Zeng; Xi-Lin Li 📂 Article 📅 2010 🏛 IEEE 🌐 English ⚖ 539 KB

P634 - DRB1 high resolution sequencing b

P634 - DRB1 high resolution sequencing based typing of 30 unrelated individuals; Comparison with PCR-SSP

✍ Daisy de Bruyn; Paul Savelkoul; Ella van den Berg-Loonen 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 167 KB

Reproducibility and validity of electric

Reproducibility and validity of electric source localisation with high-resolution electroencephalography

✍ R. Kristeva-Feige; Ch. Grimm; H.-J. Huppertz; M. Otte; A. Schreiber; D. Jäger; B 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 786 KB

The Role of Causal and Intentional Judgm

The Role of Causal and Intentional Judgments in Moral Reasoning in Individuals with High Functioning Autism

✍ Marine Buon, Emmanuel Dupoux, Pierre Jacob, Pauline Chaste, Marion Leboyer, Tizi 📂 Article 📅 2012 🏛 Springer US 🌐 English ⚖ 498 KB

TGGE screening of the entire FBN1 coding

TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

✍ Stefanie Katzke; Patrick Booms; Frank Tiecke; Monika Palz; Angelika Pletschacher 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 205 KB

Mutations in the gene for fibrillin-1 (FBN1) cause Marfan syndrome (MFS), an autosomal dominant heritable disorder of connective tissue with prominent manifestations in the skeletal, ocular, and cardiovascular system. FBN1 mutations have also been identified in a series of related disorders of conne