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Your search keyword '"Lu, Weiliang"' showing total 23 results

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23 results on '"Lu, Weiliang"'

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1. Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies

3. Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening

4. CNV profiles of Chinese pediatric patients with developmental disorders

10. Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement

12. Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome

13. Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene‐disease relationship

14. Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : evidence supporting a "Definitive" gene-disease relationship

21. A Software Design Method in the Field of Industrial Control.

22. Synthesis, characterization and magnetic properties of near monodisperse Fe3O4 sub-microspheres.

23. Loss of hnRNPA2B1 inhibits malignant capability and promotes apoptosis via down-regulating Lin28B expression in ovarian cancer.

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