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You searched for: Author/Creator Roifman, Maian

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1. Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies. (1st February 2022)

2. Genome-wide placental DNA methylation analysis of severely growth-discordant monochorionic twins reveals novel epigenetic targets for intrauterine growth restriction. Issue 1 (December 2016)

4. Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Issue 6 (1st October 2020)

6. The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?. Issue 9 (20th July 2020)