Jan. 14, 2025 — Using advanced imaging techniques and precise microfluidics control to stretch out curly DNA into a straight line, new research demonstrates techniques for stretching and ...

An abnormal development of the forebrain, holoprosencephaly, is the most common cranial abnormality in infants with Trisomy 13. The embryology and implications of holoprosencephaly are described.

Fluorescence imaging is the visualization of fluorescent dyes or proteins as labels for molecular processes or structures. It enables a wide range of experimental observations including the ...

However, a 300 kb deletion of 18p11.31, including the TGIF1 gene, was identified and is likely the cause of the holoprosencephaly seen in the fetus.