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Title:           The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype
Subject:         eBioMedicine, 78 (2022) 103952. doi:10.1016/j.ebiom.2022.103952
Keywords:        "Prader-Wlli syndrome"; "Gender specific genomic imprinting"; "Hyperphagia"; "Foetal nutritional pathways"
Author:          Anthony Holland
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      Title: The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype
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          Title: PWS as a disorder of brain development
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  Checksum: 41688054
   Type: CRC32
  Checksum: 133005149951402a1e6ba028a3032c34
   Type: MD5
  Checksum: 05e8f5dc9d972896f44e91271010e8714bddebb4
   Type: SHA-1
  Checksum: 35ba47aa2fda1d131f0796798ad5b11c46e5a0aa6d332460c70413c43906a65f
   Type: SHA-256