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Human Genetics|January 7, 1998
Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disordersM Tartaglia, C Di Rocco, E Lajeunie, et al.
Biochemical and Biophysical Research Communications|June 15, 1994
Genetic tests to reveal TAT homodimer formation and select TAT homodimer inhibitorP A Battaglia, F Longo, C Ciotta, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosisM Tartaglia, V Bordoni, F Velardi, et al.
The American Journal of Pathology|May 18, 1999
Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disordersA Fragale, M Tartaglia, S Bernardini, et al.
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