Prenatal diagnosis of Fraser syndrome using routine ultrasound examination, confirmed by exome sequencing – report of a novel homozygous missense FRAS1 mutation
Source: Congenital Anomalies - Category: Genetics & Stem Cells Authors: Jakub Kornacki, Anna Sowińska‐Seidler, Magdalena Socha, Mariola Ropacka, Aleksander Jamsheer Tags: Note Source Type: research
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