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PMID: 2328991 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.

Genomics ·Vol. 6 ·No. 3 ·1990-03-00 ·Pages 521-7

Buiting K, Neumann M, Lüdecke HJ, Senger G, Claussen U, Antich J, Passarge E, Horsthemke B

Abstract

The Prader-Willi syndrome chromosome region on the long arm of human chromosome 15 was microdissected and microcloned from 20 GTG-banded metaphase chromosomes, and 5000 recombinant clones were obtained. Of these clones, 39% identify single-copy human DNA sequences, most of which map to the dissected chromosome region and are evolutionarily conserved in other species. Three of eleven clones studied in detail are deleted in several patients with Prader-Willi syndrome. The microclones will be useful for the physical characterization of the Prader-Willi syndrome chromosome region and the identification of the affected genes in this disease.

MeSH Terms
Adult Child Child, Preschool Chromosome Aberrations/genetics Chromosome Banding Chromosome Deletion Chromosome Disorders Chromosome Inversion Chromosomes, Human, Pair 15/ultrastructure Chromosomes, Human, Pair 3/ultrastructure DNA, Recombinant Female Gene Amplification Humans Male Prader-Willi Syndrome/genetics Translocation, Genetic
Chemicals
DNA, Recombinant
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Buiting K
Institut für Humangenetik, Universitätsklinikum Essen, Federal Republic of Germany.
Neumann M
Lüdecke H J
Senger G
Claussen U
Antich J
Passarge E
Horsthemke B
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1990-03-00
Pages
521-7
Language
English
Region
United States
NLM ID
8800135
Subset
IM
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