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7. Identifying a cis-element in PtoCP1 promoter for efficiently controlling constitutive gene expression in Populus tomentosa.

9. Upward Bullying as Experienced by Chinese Nurse Managers: A Qualitative Study.

12. Carrier rate of thalassemia among 25,910 high school students in Shaoguan area, China.

13. Transnasal negative pressure therapy for accelerating healing and improving the prognosis of pharyngocutaneous fistula.

18. Performance characterization of PCR-free whole genome sequencing for clinical diagnosis

22. Performance characterization of PCR-free whole genome sequencing for clinical diagnosis

23. Validation and Depth Evaluation of Low-Pass Genome Sequencing in Prenatal Diagnosis Using 387 Amniotic Fluid Samples

26. The UK10K project identifies rare variants in health and disease

27. Deep Learning for Diagnosis and Classification of Obstructive Sleep Apnea: A Nasal Airflow-Based Multi-Resolution Residual Network

28. Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples

32. VirusDIP: Virus Data Integration Platform

33. CNSA: a data repository for archiving omics data

34. Mental health status and coping strategy of medical workers in China during The COVID-19 outbreak

36. Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

37. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

38. Design of a liver cancer-specific selector for the analysis of circulating tumor DNA

39. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

40. Clinical diagnosis of single-gene disorders and chromosomal abnormalities based on BGISEQ-500 platform

41. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

44. CNSA: a data repository for archiving omics data.

46. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

47. Identification of a disease-causing mutation in a Chinese patient with retinitis pigmentosa by targeted next-generation sequencing

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