๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15

โœ Scribed by Lut Van Laer; Guy Van Camp; Eric D. Green; Egbert H. Huizing; Patrick J. Willems

Publisher
Springer
Year
1997
Tongue
English
Weight
51 KB
Volume
99
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Acute lymphoblastic leukemia in a patien
Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes
โœ Roberto Mendoza-Londono; Catherine D. Kashork; Lisa G. Shaffer; Robert Krance; S ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 160 KB ๐Ÿ‘ 1 views

## Abstract Greig cephalopolysyndactyly (GCPS; OMIM 175700) is an autosomal dominant condition caused by mutations of the gene __GLI3__, located on 7p13. To date, several cases of deletions and/or translocations involving this locus have been reported in patients with GCPS. __GLI3__ is a transcript

The human cytochrome b5gene and two of i
The human cytochrome b5gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectively
โœ Sara J. Giordano; Min Yoo; David C. Ward; Madhvi Bhatt; Joan Overhauser; Alan W. ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Springer ๐ŸŒ English โš– 330 KB

Using very high stringency hybridization conditions for the Southern blot hybridization analysis of hamster-human cell hybrid DNA, we were able to map the human cytochrome b5 gene and two of its pseudogenes (psgb 51 and psgb52 ) unambiguously to chromosomes 18, 14, and 20. These localizations were c