Publications by authors named "Mark B Mallozzi"

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Particles Matter: Air Pollution and Disparities in Sarcoidosis.
Mark B Mallozzi, Margaret M Mroz, Lisa A Maier

Am J Respir Crit Care Med· October 2025

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ANKRD11 variants: KBG syndrome and beyond.
Ilaria Parenti, Mark B Mallozzi, Irina Hüning, Cristina Gervasini, Alma Kuechler

Clin Genet· August 2021

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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Frank J Kaiser, Morad Ansari, Diana Braunholz, María Concepción Gil-Rodríguez, Christophe Decroos, Mark B Mallozzi

Hum Mol Genet· June 2014

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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.
Diana Braunholz, Melanie Hullings, María Concepcion Gil-Rodríguez, Christopher T Fincher, Mark B Mallozzi

Eur J Hum Genet· March 2012

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