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Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion

✍ Scribed by Zori, Roberto T. ;Lupski, James R. ;Heju, Zhang ;Greenberg, Frank ;Killian, James M. ;Gray, Brian A. ;Driscoll, Daniel J. ;Patel, Pragna I. ;Zackowski, Joleen L.


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
922 KB
Volume
47
Category
Article
ISSN
0148-7299

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