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UnknownIdentification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.
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S-EPMC6683566 | biostudies-literature
UnknownLIG4 syndrome: clinical and molecular characterization in a Chinese cohort.
Not available
S-EPMC7257218 | biostudies-literature
UnknownTRIM59-mediated ferroptosis enhances neuroblastoma development and chemosensitivity through p53 ubiquitination and degradation.
Not available
S-EPMC10906161 | biostudies-literature
UnknownDietary folic acid intake, 13 genetic variants and other factors with red blood cell folate concentration in pregnancy-preparing population.
Not available
S-EPMC11519176 | biostudies-literature
UnknownRBC transfusion and necrotizing enterocolitis in very preterm infants: a multicenter observational study.
Not available
S-EPMC11192881 | biostudies-literature
UnknownCopy number variant analysis for syndromic congenital heart disease in the Chinese population.
Not available
S-EPMC9623925 | biostudies-literature
UnknownAdverse Reaction Reporting for Naxitamab in Chinese Expanded Access Treatment for Relapsed/Refractory High-Risk Neuroblastoma at the Children's Hospital of Fudan University.
Not available
S-EPMC11829859 | biostudies-literature
UnknownA splicing variation in NPRL2 causing familial focal epilepsy with variable foci: additional cases and literature review.
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S-EPMC8786660 | biostudies-literature
UnknownNext-Generation Sequencing-Based Copy Number Variation Analysis in Chinese Patients with Primary Ciliary Dyskinesia Revealed Novel DNAH5 Copy Number Variations.
Not available
S-EPMC11003934 | biostudies-literature
UnknownFeeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Not available
S-EPMC6543684 | biostudies-literature
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