,:

Bárbara Braga Vieira Marques1, Ingrid Souza Dias2, Amanda Cristina Meneguetti Berti1

  • 1São Paulo State University (UNESP), Institute of Biosciences, Humanities and Exact Sciences, Bioscience Postgraduate Program, São José do Rio Preto, SP, Brazil; Federal University of Mato Grosso do Sul (UFMS), Molecular Biology and Genetics Laboratory, Três Lagoas, MS, Brazil.

Clinical biochemistry
|March 1, 2025
PubMed
概括

诊断复杂的血红蛋白病症需要先进的分子技术. 这一案例凸显了理解全球链遗传学对于新生儿结合Hb C/Beta0血病和Hb B2共同遗传的准确诊断的重要性.