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Mei Chi Cheung

Researcher at University of California, San Francisco

Publications -  5
Citations -  488

Mei Chi Cheung is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Chromosome 21 & Chromosome 22. The author has an hindex of 5, co-authored 5 publications receiving 483 citations.

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High-Resolution Chromosome Sorting and DNA Spot-Blot Analysis Assign McArdle's Syndrome to Chromosome 11

TL;DR: A rapid gene-mapping system uses a high-resolution, dual-laser sorter to identify genes from separate human chromosomes prepared with a new stain combination to sort 21 unique chromosome types onto nitrocellulose filter papers.
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cDNA sequence for human erythrocyte ankyrin.

TL;DR: The cDNA for human erythrocyte ankyrin has been isolated from a series of overlapping clones obtained from a reticulocyte cDNA library, and two cDNA clones showed evidence of apparent mRNA processing, resulting in deletions of 486 bp and 135 bp.
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Construction of human chromosome 21-specific yeast artificial chromosomes

TL;DR: YACs have been constructed by a method that performs all steps in agarose, allowing size selection by pulsed-field gel electrophoresis and the use of nanogram to microgram quantities of DNA.
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Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sorting.

TL;DR: Simultaneous sorting of the normal homolog from this small derivative chromosome separated the two different sized insulin gene-containing restriction fragments in this individual, indicating that the two restriction fragments represent insulin gene polymorphism and not duplicate gene loci.
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Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19.

TL;DR: In order to map human PGKsequences, DNA was prepared from 55 human-mouse somatic cell lines and hybridized to flow-sorted chromosomes confirming the presence of PGK sequences on the X chromosome and chromosomes 6 and 19.