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- W2078744499 abstract "We have found fluorescence in situ hybridization (FISH) results more reliavle than high resolution chromosome analysis for the diagnosis of Prader-Willi (PWS) or Angelman syndromes (AS). Specifically, we have found success in the detection of 15q11q13 deletions among 55 cases. Our study suggests that FISH analysis using PWS/AS probes can facilitate diagnostic evaluation of these cases for deletions. 2 refs., 1 tab." @default.
- W2078744499 created "2016-06-24" @default.
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- W2078744499 date "1995-07-01" @default.
- W2078744499 modified "2023-09-27" @default.
- W2078744499 title "Fluorescent in situ hybridization for evaluation of prader-willi and angelman syndromes" @default.
- W2078744499 cites W1977782433 @default.
- W2078744499 doi "https://doi.org/10.1002/ajmg.1320570426" @default.
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- W2078744499 hasPublicationYear "1995" @default.
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