✦ LIBER ✦

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

✍ Scribed by G. Poelmans; J.J.M. Engelen; J. Van Lent-Albrechts; H.J. Smeets; E. Schoenmakers; B. Franke; J.K. Buitelaar; M. Wuisman-Frerker; W. Erens; J. Steyaert; C. Schrander-Stumpel

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 233 KB
Volume: 150B
Category: Article
ISSN: 1552-4841
DOI: 10.1002/ajmg.b.30787

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of three 11p11.2 candidat

Identification of three 11p11.2 candidate liver tumor suppressors through analysis of known human genes

✍ Sharon L. Ricketts; Jennifer C. Carter; William B. Coleman 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 186 KB

## Abstract We have previously mapped a liver tumor suppressor locus to human chromosome 11p11.2‐p12 using a functional model of tumor suppression. Using this model system, we have employed a candidate gene approach to identify potential liver tumor suppressor genes. Thirty‐eight known genes have b

Molecular analysis of nonrandom 8q12 del

Molecular analysis of nonrandom 8q12 deletions in acute lymphoblastic leukemia: Identification of two candidate genes

✍ Valérie Bardet; Nathalie Couque; Laurence Cattolico; Gilles Hetet; Isabelle Deva 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 194 KB

## Abstract Acute lymphoblastic leukemia is the most common malignancy in childhood. High‐resolution allelotyping performed in our laboratory showed new chromosomal sites of nonrandom deletions. We have focused our work on 8q12 deletions, which we have found in about 4% of patients (eight of 205 in

Disruption of sixSaccharomyces cerevisia

Disruption of sixSaccharomyces cerevisiae novel genes and phenotypic analysis of the deletants

✍ Zúñiga, Sonia; Boskovic, Jasminka; Jiménez, Antonio; Ballesta, Juan P. G.; Remac 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 303 KB 👁 2 views

As a part of the EUROFAN programme, six open reading frames from Saccharomyces cerevisiae (YNL083w, YNL086w, YNL087w, YNL097c, YDL100c and YOR086c) were disrupted in two genetic backgrounds, FY1679 and W303. Individual deletions in diploid strains and tetrad analysis of heterozygous deletants reveal

Candidate gene analysis in Rett syndrome

Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq

✍ Amir, Ruthie; Dahle, E. Jill Roth; Toriolo, Daniela; Zoghbi, Huda Y. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 17 KB 👁 2 views

Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder that affects females. Exclusion mapping studies using a new family with maternal inheritance of RTT defined Xq28 as the candidate region for the RTT gene. Six candidate genes were selected for mutation analysis based on their es

Analysis of the NF2 tumor-suppressor gen

Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas

✍ Khě Hoano-Xuan; Philippe Meree; Felipe Vega; Jean-Pierre Hugot; Philippe Cornu; 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 652 KB

## Abstract Recurrent deletions of chromosome fragments observed in neoplasms are thought to participate in tumor development through the inactivation of tumor‐suppressor genes. In gliomas, the most frequent deletions involve chromosome arms 9p, 10q, 17p, 19q and 22q. We have analysed deletions of

FISH analysis for apparently simple term

FISH analysis for apparently simple terminal deletions of the X chromosome: Identification of hidden structural abnormalities

✍ Ogata, Tsutomu ;Matsuo, Nobutake ;Fukushima, Yoshimitsu ;Saito, Masakazu ;Nose, 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB

We report on ¯uorescence in situ hybridization (FISH) analysis in 30 mosaic or nonmosaic females diagnosed as having apparently simple terminal X deletions by standard G-banding analysis. FISH studies for DXZ1, the Xp and Xq telomere regions, and the whole X chromosome painting were carried out for