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About this Biochemistry, Genetics and Molecular Biology article

Chromosome deletion 17pl 1.2 (Smith‐Magenis syndrome) in seven new patients, four of whom had been referred for fragile‐X investigation by F. Behjati; M. Mullarkey; A. Bergbaum; A. C. Berry; Z. Docherty 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
F. Behjati; M. Mullarkey; A. Bergbaum; A. C. Berry; Z. Docherty
Publisher
John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
Published
2008
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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