Severe trichothiodystrophy and cardiac malformation in a newborn carrying a novel GTF2H5 homozygous truncating variant.

MLA

Sorrentino, Ugo, et al. “Severe Trichothiodystrophy and Cardiac Malformation in a Newborn Carrying a Novel GTF2H5 Homozygous Truncating Variant.” Clinical Genetics, vol. 104, no. 5, Nov. 2023, pp. 604–06. EBSCOhost, https://doi.org/10.1111/cge.14396.

APA

Sorrentino, U., Agosto, C., Benini, F., Bertolin, C., Cassina, M., Bonadies, L., Caroppo, F., Fortina, A. B., & Salviati, L. (2023). Severe trichothiodystrophy and cardiac malformation in a newborn carrying a novel GTF2H5 homozygous truncating variant. Clinical Genetics, 104(5), 604–606. https://doi.org/10.1111/cge.14396

Chicago

Sorrentino, Ugo, Caterina Agosto, Franca Benini, Cinzia Bertolin, Matteo Cassina, Luca Bonadies, Francesca Caroppo, Anna Belloni Fortina, and Leonardo Salviati. 2023. “Severe Trichothiodystrophy and Cardiac Malformation in a Newborn Carrying a Novel GTF2H5 Homozygous Truncating Variant.” Clinical Genetics 104 (5): 604–6. doi:10.1111/cge.14396.