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Prader-Willi syndrome : genetic disorder, chromosome 15 (human), chromosome 15q partial deletion, Guido Fanconi, Angelman syndrome, genomic imprintin, hypotonia Preview this item
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Prader-Willi syndrome : genetic disorder, chromosome 15 (human), chromosome 15q partial deletion, Guido Fanconi, Angelman syndrome, genomic imprintin, hypotonia

Author: Lambert M Surhone; Mariam T Tennoe; Susan F Henssonow
Publisher: [S.l.] : Betascript Pub., 2010.
Edition/Format:   Book : English
Database:WorldCat
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Document Type: Book
All Authors / Contributors: Lambert M Surhone; Mariam T Tennoe; Susan F Henssonow
OCLC Number: 727363183
Notes: "All parts of this book are extracted from Wikipedia, the free encyclopedia (www.wikipedia.org)."--T.p. verso.
Publisher contact: VDM Publishing House Ltd., 17 Rue Meldrum, Beau Bassin, 1713-01 Mauritius. www.vdm-publishing-house.com.
Description: 113 p. : ill. ; 24 cm.
Responsibility: Lambert M. Surhone, Mariam T. Timpledon, Susan F. Marseken (Ed.).

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