Genetic Manifestations and Phenotype Spectrum in Infants With Feeding Difficulty.

Mingyu HanWei ShiXiangxiang ChenDingwen WuYi SunWeiyan WangCanyang ZhanLingling HuTianming Yuan

Published in: Molecular genetics & genomic medicine (2024)

Feeding difficulty may constitute a facet of the phenotypic spectrum of rare genetic diseases. Whole-exome sequencing can enhance molecular diagnosis accuracy for infants with feeding difficulties.

Keyphrases

genome wide
gene expression
dna methylation