Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation. (Q53602612)
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scientific article
Language | Label | Description | Also known as |
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English | Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation. |
scientific article |
Statements
Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation (English)
Marcelo Valente
Kette D Valente
Sofia S M Sugayama