✦ LIBER ✦

Gene–based sequence–tagged–sites (STSs) as the basis for a human gene map

✍ Scribed by Berry, Rebecca; Stevens, T.J.; Walter, Nicole A.R.; Wilcox, Andrea S.; Rubano, Todd; Hopkins, Janet A.; Weber, James; Goold, Richard; Soares, Marcelo Bento; Sikela, James M.

Book ID: 109916696
Publisher: Nature Publishing Group
Year: 1995
Tongue: English
Weight: 678 KB
Volume: 10
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng0895-415

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

An intraspecific linkage map of the chic

An intraspecific linkage map of the chickpea (Cicer arietinumL.) genome based on sequence tagged microsatellite site and resistance gene analog markers

✍ H. Flandez-Galvez; R. Ford; E. C. K. Pang; P. W. J. Taylor 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 244 KB

Mapping the limits of the human pseudoau

Mapping the limits of the human pseudoautosomal region and a candidate sequence for the male-determining gene

✍ Pritchard, Catrin A.; Goodfellow, Paul J.; Goodfellow, Peter N. 📂 Article 📅 1987 🏛 Nature Publishing Group 🌐 English ⚖ 369 KB

A Random DNA Sequencing, Computer-Based

A Random DNA Sequencing, Computer-Based Approach for the Generation of a Gene Map of Molluscum Contagiosum Virus

✍ ANTONIO J Varas; MARIANO Esteban; MARTA Moratilla; MONICA Agromayor†; ANTONIA Ma 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 147 KB

Single base-pair substitutions at the tr

Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease

✍ Andreas Wolf; Amke Caliebe; Nick S.T. Thomas; Edward V. Ball; Matthew Mort; Pete 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 236 KB

A total of 405 unique single base-pair substitutions, located within the ATG translation initiation codons (TICs) of 255 different genes, and reported to cause human genetic disease, were retrieved from the Human Gene Mutation Database (HGMD). Although these lesions comprised only 0.7% of coding seq

The human neuregulin-2 (NRG2) gene: clon

The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q

✍ H. Z. Ring; H. Chang; Angèle Guilbot; Alexis Brice; Eric LeGuern; Uta Francke 📂 Article 📅 1999 🏛 Springer 🌐 English ⚖ 228 KB