## Abstract Deletion 3p syndrome is associated with characteristic facial features, growth failure, and mental retardation. Typically, individuals with deletion 3p syndrome have terminal deletions that result in loss of material from 3p25 to 3pter. We present a child with a clinical phenotype consi
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
✍ Scribed by Thomas V. Fernandez; I.J. García-González; Christopher E. Mason; G. Hernández-Zaragoza; V.C. Ledezma-Rodríguez; V.M. Anguiano-Alvarez; R. E'Vega; M. Gutiérrez-Angulo; M.L. Maya; H.E. García-Bejarano; M. González-Cruz; S. Barrios; R. Atorga; M.G. López-Cardona; J. Armendariz-Borunda; Matthew W. State; Nory O. Dávalos
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 191 KB
- Volume
- 146A
- Category
- Article
- ISSN
- 1552-4825
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## Abstract A review of the 17 previously reported cases of duplication 3p and study of a new patient who has a duplication of the chromosome segment 3p21→pter show a remarkably consistent phenotype among these patients and suggest some generalizations about prognosis. The manifestations include lo