Publications by authors named "M Baffico"

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SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators.
Silvia Vannelli, Maria Baffico, Raffaele Buganza, Francesca Verna, Giulia Vinci

Ital J Pediatr· November 2020

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Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short stature.
David J Bunyan, Maria Baffico, Lucia Capone, Silvia Vannelli, Lorenzo Iughetti

Am J Med Genet A· April 2016

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A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome.
Nicoletta Locuratolo, M Baffico, M Baldi, V Parisi, F Micacchi

Arch Ital Biol· September 2011

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Germline mosaicism in achondroplasia detected in sperm DNA of the father of three affected sibs.
Federica Natacci, Maria Baffico, Ugo Cavallari, Maria Francesca Bedeschi, Isabella Mura

Am J Med Genet A· March 2008

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FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
P Prontera, A Sensi, G Pilu, M Baldi, M Baffico

Genet Couns· May 2007

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