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RT @FrontGenetics: New Research: Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL…
RT @FrontGenetics: New Research: Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL…
New Research: Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome: Cornelia de Lange syndrome (CdLS) is a genetically heterogeneous disorder… https://t.co/johC