𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22

✍ Scribed by Elisabeth Göttert; Reinhold Metzdorf; Uwe Färber; Nikolaus Blin


Publisher
Springer
Year
1989
Tongue
English
Weight
462 KB
Volume
81
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A deletion panel of the long arm of the
✍ H. -M. Yang; T. Lund; E. Niebuhr; S. Nørby; M. Schwartz; L. Shen 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 761 KB

Two males and two females with different but overlapping deletions on the proximal long arm of the X chromosomes have been investigated. Their karyotypes, which have been well characterized by high resolution banding techniques, are 46,Y,del(X)(pter----q21.1::q21.33----qter); 46,Y,del(X)(pter----q21

Molecular genetic analysis of chromosome
✍ Markus S. von Haken; Eileen C. White; Laleh Daneshvar-Shyesther; Sharon Sih; Eug 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 644 KB

Ependymomas are glial tumors of the brain and spinal cord occurring both sporadically and in a familial syndrome, neurofibromatosis type 2 (NF2). Previous analyses performed on specimens obtained predominantly from adult patients have shown loss of DNA sequences from chromosome arm 22q, which is the

Regional localization of polymorphic DNA
✍ M. Schwartz; H. -M. Yang; E. Niebuhr; T. Rosenberg; D. C. Page 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 610 KB

In two unrelated families, males have been identified who suffer from choroideremia and at the same time have an interstitial deletion on the proximal long arm of the X chromosome. By high-resolution banding we have characterized the deletion chromosomes as del(X)(q21.1-q21.33) and del(X)(q21.2-q21.

Loss of heterozygosity on the long arm o
✍ Norifumi Tanaka; Isamu Nishisho; Masayuki Yamamoto; Akihiro Miya; Eisei Shin; Ka 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 423 KB

## Abstract To identify the putative common deleted region on the long arm of chromosome 22 in pheochromocytoma, restriction fragment length polymorphism analysis was performed in 17 pheochromocytomas. All cases were heterozygous for at least one of the eight marker loci on 22q. Loss of heterozygos

Regional localization of the phosphoglyc
✍ H. F. Willard; S. J. Goss; M. T. Holmes; D. L. Munroe 📂 Article 📅 1985 🏛 Springer 🌐 English ⚖ 584 KB

We have used a cDNA clone for human phosphoglycerate kinase (PGK) to examine the chromosomal localization of three members of the human PGK gene family. Using somatic cell hybrids segregating portions of several X-autosome translocations as well as a clone panel of hybrids segregating radiation-indu