Article Versions Notes

Dawidziuk M, Kutkowska-Kazmierczak A, Bukowska-Olech E, Jurek M, Kalka E, Guilbride DL, Furmanek MI, Bekiesinska-Figatowska M, Bal J, Gawlinski P. De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser–Winter Syndrome. International Journal of Molecular Sciences. 2022; 23(2):692. https://doi.org/10.3390/ijms23020692

Dawidziuk, Mateusz, Anna Kutkowska-Kazmierczak, Ewelina Bukowska-Olech, Marta Jurek, Ewa Kalka, Dorothy Lys Guilbride, Mariusz Ireneusz Furmanek, Monika Bekiesinska-Figatowska, Jerzy Bal, and Pawel Gawlinski. 2022. "De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser–Winter Syndrome" International Journal of Molecular Sciences 23, no. 2: 692. https://doi.org/10.3390/ijms23020692

Dawidziuk, M., Kutkowska-Kazmierczak, A., Bukowska-Olech, E., Jurek, M., Kalka, E., Guilbride, D. L., Furmanek, M. I., Bekiesinska-Figatowska, M., Bal, J., & Gawlinski, P. (2022). De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser–Winter Syndrome. International Journal of Molecular Sciences, 23(2), 692. https://doi.org/10.3390/ijms23020692