Browsing "Medical Genetics" by Keyword : Infant, Newborn

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Showing results 7 to 10 of 10

Pub YearTitleAuthor(s)
2010De novo pericentric inversion of chromosome 9 in congenital anomaly.정선용
2015Disease-specific growth charts for Korean infants with Prader-Willi syndrome.손영배
2020Loss of Heterozygosity at Chromosome 16q Is a Negative Prognostic Factor in Korean Pediatric Patients with Favorable Histology Wilms Tumor: A Report of the Korean Pediatric Hematology Oncology Group (K-PHOG)노오규, 박준은, 이용희, 정선용
1998Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation.김현주
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