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A G-band study of chromosomes in liveborn infants
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Mosaic inversion duplication of chromosome 15 without phenotypic effect: Occurrence in a father and daughter
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An extra inic(15p)(q11) chromosome in Prader-Willi syndrome
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Chromosome 15 abnormalities and the Prader-Willi syndrome: A follow-up report of 40 cases
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Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients
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Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications
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Molecular cloning and chromosomal localization of the human alpha 7-nicotinic receptor subunit gene (CHRNA7)
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High-resolution mapping of the gamma-aminobutyric-acid receptor subunit-beta-3 and alpha-5 gene-cluster on chromosome-15q11-q13, and localization of breakpoints in 2 Angelman syndrome patients
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