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Unveiling a rare genetic aberration: A case study of Prader-Willi syndrome (PWS) with atypical 15q11.2-q13.3 deletion
Published 2025-05-01Subjects: Get full text
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Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing
Published 2025-07-01Subjects: Get full text
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