Ulnar–mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.
| Autor: | Klopocki, Eva1 eva.klopocki@charite.de, Neumann, Luitgard M.2, Tönnies, Holger2, Ropers, Hans-Hilger3, Mundlos, Stefan1, Ullmann, Reinhard3 |
|---|---|
| Zdroj: | European Journal of Human Genetics. Dec2006, Vol. 14 Issue 12, p1274-1279. 6p. 1 Black and White Photograph, 2 Diagrams. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
|