Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe-Reference-Cited by-同舟云学术

Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe

Published:1991-10 Issue:2 Volume:11 Page:455-458
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Gaughan Glen,Park Heidi,Priddle John,Craig Ian,Craig Sally

Publisher

Elsevier BV

Subject

Genetics

Reference13 articles.

1. Gene dosage effect present in trisomy 3q25.2-qter for serum cholinesterase (CHE1) and absent for transferrin (TF) and ceruloplasmin (CP);Arias;Cytogenet. Cell Genet,1985

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

3. In situ hybridisation;Buckle,1986

4. Localisation of neurone-specific enolase (ENO2) to 12q13;Craig;Cytogenet. Cell Genet,1990

5. Genetical studies on a new variant of serum cholinesterase detected by electrophoresis;Harris;Ann. Hum. Genet,1963

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