Associated Papers
Malformations of cortical development: Fetal imaging and genetics.
Wang LL et al.
Molecular Genetics & Genomic Medicine, 2024
Compound variants of FKTN, POMGNT1, and LAMB1 gene identified by prenatal whole-exome sequencing in three fetuses with congenital hydrocephalus.
Li M et al.
The Journal of Obstetrics and Gynaecology Research, 2022
Fetal phenotypes of Mendelian disorders: A descriptive study from India.
Saini N et al.
Prenatal Diagnosis, 2022
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