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Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function by Tooze, RS, Calpena, E, Twigg, SRF, D'Arco, F, Wakeling, EL, Wilkie, AOM
Published 2022Journal article -
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BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations by Peron, A, D’Arco, F, Aldinger, KA, Smith-Hicks, C, Zweier, C, Gradek, GA, Bradbury, K, Accogli, A, Andersen, EF, Au, PYB, Battini, R, Beleford, D, Bird, LM, Bouman, A, Bruel, A, Busk, ØL, Campeau, PM, Capra, V, Carlston, C, Carmichael, J, Chassevent, A, Clayton-Smith, J, Bamshad, MJ, Earl, DL, Shears, D
Published 2024Journal article