Incidental detection of a chromosomal aberration by array-cgh in an early prenatal diagnosis for monogenic disease on coelomic fluid

HIGHLIGHTS

• who: Margherita Vinciguerra and collaborators from the Sofia-Cervello, Palermo, Italy have published the article: Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid, in the Journal: Life 2022, 12, x FOR PEER REVIEW of /2022/
• what: The authors report a case of monosomy X detected during a prenatal diagnosis for beta thalassemia on fluid (CF) at the VIII week of gestation.
• future: The application of this technology on coelomic fluid in the field of prenatal diagnosis has shown that this methodology . . .
  

   

  

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