Mapping the human acetylcholinesterase gene to chromosome 7q22 by fluorescent in situ hybridization coupled with selective PCR amplification from a somatic hybrid cell panel and chromosome-sorted DNA libraries-Reference-Cited by-同舟云学术

Mapping the human acetylcholinesterase gene to chromosome 7q22 by fluorescent in situ hybridization coupled with selective PCR amplification from a somatic hybrid cell panel and chromosome-sorted DNA libraries

Published:1992-08 Issue:4 Volume:13 Page:1192-1197
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Ehrlich Gal,Viegas-Pequignot Evani,Ginzberg Dalia,Sindel Lilian,Soreq Hermona,Zakut Haim

Publisher

Elsevier BV

Subject

Genetics

Reference24 articles.

1. Structure of the gene for human butyrylcholinesterase: Evidence for a single copy;Arpagaus;Biochemistry,1990

2. A neural tube defect specific form of acetylcholinesterase in amniotic fluid;Bonham;Clin. Chem. Acta,1983

3. Genetic variation in human erythrocyte acetylcholinesterase;Coates;Science,1972

4. Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes;Deavan,1986

5. Expression of alternatively terminated unusual human butyrylcholinesterase messenger RNA transcripts, mapping to chromosome 3q26-ter, in nervous system tumors;Gnatt;Cancer Res,1990

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