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Studies of TBX4 and chromosome 17q23.1q23.2: An uncommon cause of nonsyndromic clubfoot

✍ Scribed by W. Lu; C.A. Bacino; B.S. Richards; C. Alvarez; J.E. VanderMeer; M. Vella; N. Ahituv; N. Sikka; F.R. Dietz; S.H. Blanton; J.T. Hecht


Book ID
111995240
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
464 KB
Volume
158A
Category
Article
ISSN
1552-4825

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Microdeletion of 17q22q23.2 encompassing
✍ Manjunath Nimmakayalu; Heather Major; Val Sheffield; Donald H. Solomon; Richard πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 288 KB

## Abstract Microdeletions of the long arm of chromosome 17 are being reported with increasing frequency. Deletions of 17q22q23.2 may represent a genetically recognizable phenotype although its spectrum of genomic abnormalities, clinical manifestations, and critical regions are not fully delineated