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https://www.selleckchem.com/MEK.html
OBJECTIVE To explore the genetic basis for a child with autism spectrum disorder (ASD) and congenital heart disease. METHODS G-banded chromosomal karyotyping was carried out for the patient and his parents. The child was also subjected to whole exome sequencing (WES) and low-coverage massively parallel copy number variation sequencing (CNV-seq). The result was validated by chromosomal microarray analysis (CMA). RESULTS The karyotype of the patient and his parents were normal. No significant genetic variation was found by WES. However, CNV-seq has di

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