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Naslov: Whole exome sequencing diagnoses the first fetal case ofBainbridge‐Ropers syndrome presenting as pontocerebellar hypoplasia type 1
Vir:

Birth defects research [Birth Defects Res] NLMUID [2472-1727] Bacrot, Séverine l. 2018, letn. 110, št. 6, str. 538 -542

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