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About this Biochemistry, Genetics and Molecular Biology article
Prader–Willi syndrome phenocopy due to duplication of Xq21.1–q21.31, with array CGH of the critical region by MT Gabbett; GB Peters; JM Carmichael; AP Darmanian; FA Collins is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- MT Gabbett; GB Peters; JM Carmichael; AP Darmanian; FA Collins
- Publisher
- John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
- Published
- 2008
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)
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