A family with nine siblings showing signs of Rothmund–Thomson syndrome with two being definitely diagnosed with the syndrome due to homozygous N‐terminal mutation of RECQL4.

MLA

Yadegari, Fatemeh, et al. “A Family with Nine Siblings Showing Signs of Rothmund–Thomson Syndrome with Two Being Definitely Diagnosed with the Syndrome Due to Homozygous N‐terminal Mutation of RECQL4.” Clinical Case Reports, vol. 12, no. 8, Aug. 2024, pp. 1–6. EBSCOhost, https://doi.org/10.1002/ccr3.9176.

APA

Yadegari, F., Abed, A. R., Abd, A. W. Y., Al, A. H. H., Zarinfam, S., Aminian, S., & Majidzadeh, A. K. (2024). A family with nine siblings showing signs of Rothmund–Thomson syndrome with two being definitely diagnosed with the syndrome due to homozygous N‐terminal mutation of RECQL4. Clinical Case Reports, 12(8), 1–6. https://doi.org/10.1002/ccr3.9176

Chicago

Yadegari, Fatemeh, Aseel Rashid Abed, Ali, Widad Yadallah Abd, Abedi, Haider Hamza Al, Shiva Zarinfam, Solaleh Aminian, and A, Keivan Majidzadeh. 2024. “A Family with Nine Siblings Showing Signs of Rothmund–Thomson Syndrome with Two Being Definitely Diagnosed with the Syndrome Due to Homozygous N‐terminal Mutation of RECQL4.” Clinical Case Reports 12 (8): 1–6. doi:10.1002/ccr3.9176.