Lilach Benyamini
Shamir, Z, Israel
Last Updated: 09/26/2026
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Found 8 publications
Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: January 27, 2025
Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.
Journal: Journal of medical genetics
Published: July 10, 2023
Simple Evaluation of Thyroid Function Leading to the Diagnosis of Allan-Herndon-Dudley Syndrome, a Rare Neurodevelopmental Disorder.
Journal: The Israel Medical Association journal : IMAJ
Published: May 28, 2023
Novel perspectives of super-high dose sulfonylurea and high-dose oral prednisolone in an infant with DEND syndrome due to V64M heterozygote KCNJ11 mutation.
Journal: Acta diabetologica
Published: March 13, 2021
Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.
Journal: Journal of perinatal medicine
Published: October 17, 2017
A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.
Journal: Human mutation
Published: September 10, 2015
Congenital myopathy is caused by mutation of HACD1.
Journal: Human molecular genetics
Published: August 13, 2013
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Last Updated: 09/26/2026