Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints
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DOI: 10.1002/mgg3.806
Abstract: Here, we report the prenatal detection of a compound heterozygous deletion at chromosome 15q15.3 by clinical chromosomal microarray (CMA) testing that included the CATSPER2 male infertility gene. However, given the low resolution of CMA at… read more here.
Keywords: identification molecular; prenatal cytogenomic; deletion; cytogenomic identification ... See more keywords