DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

Referenz

Pariani MJ, Spencer A, Graham Jr JM, Rimoin DLA.
A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis.

Eur J Med Genet 2009;
52 (2-3): 123-127

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