| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4142288 | Anales de Pediatría | 2011 | 4 Pages |
Abstract
We describe the case of a newborn female with polysyndactyly, hypertelorism and microcephaly and a 1.5 Mb 7p14.1 microdeletion of paternal origin diagnosed by array-CGH.
Keywords
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Authors
D. Montoro Cremades, I. Manchón Trives, V. Botella López, L. Alcaraz Más, M.R. GarcÃa MartÃnez, F. Galán Sánchez,