Importance and application of WES in fetal genetic diagnostics: Identification of novel ASPM mutation in a fetus with microcephaly. Mol Genet Metab Rep. 2024 Jan 18;38:101056. doi: 10.1016/j.ymgmr.2024.101056. PMID: 38469100; PMCID: PMC10926227.

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Omikai Központ Pécs > Blog > 2024 > Importance and application of WES in fetal genetic diagnostics: Identification of novel ASPM mutation in a fetus with microcephaly. Mol Genet Metab Rep. 2024 Jan 18;38:101056. doi: 10.1016/j.ymgmr.2024.101056. PMID: 38469100; PMCID: PMC10926227.

ducsaba október 22, 2025 Nincs hozzászólás

Importance and application of WES in fetal genetic diagnostics: Identification of novel ASPM mutation in a fetus with microcephaly. Mol Genet Metab Rep. 2024 Jan 18;38:101056. doi: 10.1016/j.ymgmr.2024.101056. PMID: 38469100; PMCID: PMC10926227.

Szalai R, Till A, Gyenesei A, Bene J, Hadzsiev K.

Importance and application of WES in fetal genetic diagnostics: Identification of novel ASPM mutation in a fetus with microcephaly. Mol Genet Metab Rep. 2024 Jan 18;38:101056. doi: 10.1016/j.ymgmr.2024.101056. PMID: 38469100; PMCID: PMC10926227.

Glioblastoma epigenomics discloses a complex biology and potential therapeutic targets. Ideggyogy Sz. 2024 Jan 30;77(1-2):27-37. English. doi: 10.18071/isz.77.0027. PMID: 38321856.

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