𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mapping of gene loci in the Q13–Q15 region of chromosome 12

✍ Scribed by Erika L. D. Mitchell; Gavin R. M. White; Mauro F. Santibanez-Koref; Jenny M. Varley; Jim Heighway

Publisher
Springer
Year
1995
Tongue
English
Weight
212 KB
Volume
3
Category
Article
ISSN
0967-3849

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Transmission disequilibrium testing of t
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism
✍ Soo-Jeong Kim; Camille W. Brune; Emily O. Kistner; Susan L. Christian; Eric H. C 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 153 KB 👁 1 views

## Abstract Evidence implicates the serotonin transporter gene (__SLC6A4__) and the 15q11‐q13 genes as candidates for autism as well as restricted repetitive behavior (RRB). We conducted dense transmission disequilibrium mapping of the 15q11‐q13 region with 93 single nucleotide polymorphisms (SNPs)

Partial linkage map of chromosome 13q in
Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes
✍ Jonathan L. Haines; Laurie Ozelius; Peter St George-Hyslop; Nancy S. Wexler; Jam 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 345 KB

Genetic linkage maps are useful tools for defining the location of disease genes. Previously published maps of human chromosome 13 have been incomplete and have had ambiguities of order in the vicinity of the Wilson disease (WND) and retinoblastoma (RB1) genes. We have defined a six-locus map of thi

Interstitial duplications of chromosome
Interstitial duplications of chromosome region 15q11q13: Clinical and molecular characterization
✍ Repetto, Gabriela M.; White, Lisa M.; Bader, Patricia J.; Johnson, Debra; Knoll, 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 45 KB 👁 2 views

D u p l i c a t i o n s o f c h r o m o s o m e r e g i o n 15q11q13 often occur as a supernumerary chromosome 15. Less frequently they occur as interstitial duplications [dup(15)]. We describe the clinical and molecular characteristics of three patients with de novo dup(15). The patients, two males

Mapping of the ribophorin II (RPN II) ge
Mapping of the ribophorin II (RPN II) gene to human chromosome 20q12–q13.1 by in-situ hybridization
✍ Christiane Löffler; V. V. N. Gopal Rao; Ingo Hansmann 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 187 KB

Ribophorin I and II (RPN I and RPN II), two specific glycoproteins, span the rough regions of the endoplasmic reticulum (RER) and are thought to play an important role either in translocation or in the maintenance of RER. Studies with human-mouse somatic cell hybrids have localized the gene for RPN

Deletion of chromosome 11p15, p12, q22,
Deletion of chromosome 11p15, p12, q22, q23-24 loci in human prostate cancer
✍ Rajvir Dahiya; Joseph McCarville; Celeste Lee; Weixing Hu; Gurjit Kaur; Peter Ca 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 French ⚖ 126 KB 👁 1 views

Loss of heterozygosity (LOH) on chromosome 11 is frequently altered in various epithelial cancers. The present study was designed to investigate LOH on chromosome 11 in microdissected samples of normal prostatic epithelium and invasive carcinoma from the same patients. For this purpose, DNA was extr