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- W4248364953 abstract "We report on an additional fourth case of Prader–Willi (PW)-like phenotype and an interstitial deletion of 6q. Despite sharing clinical characteristics, patients with a PW-like phenotype and a deletion of 6q, have features which distinguish them from Prader–Willi syndrome (PWS) patients. This case emphasizes the need to examine patients with suspected PWS, but who are negative for recognizable deletions of 15q11–q13 or uniparental maternal disomy of chromosome 15, for a deletion of 6q." @default.
- W4248364953 created "2022-05-12" @default.
- W4248364953 date "1994-04-01" @default.
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- W4248364953 title "Author Index for Volume 146" @default.
- W4248364953 doi "https://doi.org/10.1006/jcat.1994.1107" @default.
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