25 results on '"Du, Caiqi"'
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2. Xq26.3-q27.1 duplication including SOX3 gene in a Chinese boy with hypopituitarism: case report and two years treatment follow up
3. Intrauterine inflammation induced white matter injury protection by fibrinogen-like protein 2 deficiency in perinatal mice
4. Clinical analysis and long-term treatment monitoring of 3 patients with glycogen storage disease type Ib
5. Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia
6. A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family
7. Prevalence of vitamin D deficiency in girls with idiopathic central precocious puberty
8. Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children
9. Corrigendum to CO suppresses prostate cancer cell growth by directly targeting LKB1/AMPK/m-TOR pathway in vitro and in vivo
10. CO suppresses prostate cancer cell growth by directly targeting LKB1/AMPK/mTOR pathway in vitro and in vivo
11. Case Report: Glycogen Storage Disease Type Ia in a Chinese Child Treated With Growth Hormone
12. Additional file 3 of Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia
13. Additional file 1 of Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia
14. Analysis of the Screening Results for Congenital Adrenal Hyperplasia Involving 7.85 Million Newborns in China: A Systematic Review and Meta-Analysis
15. Clinical Analysis and Long-term Treatment Monitoring of 3 Patients with Glycogen Storage Disease Type Ib
16. Intrauterine inflammation induced white matter injury protection by fibrinogen-like protein 2 deficiency in perinatal mice
17. Genotypic and clinical analysis of 49 Chinese children with hepatic glycogen storage diseases
18. Genetic analysis and long-term treatment monitoring of 11 children with glycogen storage disease type IIIa
19. Novel truncating variant of PPM1D penultimate exon in a Chinese patient with Jansen‐de Vries syndrome
20. Decreased Circulating Levels of Asprosin in Obese Children
21. Characterization of fibroblast growth factor 1 in obese children and adolescents
22. Circulating MOTS-c levels are decreased in obese male children and adolescents and associated with insulin resistance
23. Prevalence of vitamin D deficiency in girls with idiopathic central precocious puberty
24. Increased Cord Blood Betatrophin Levels in the Offspring of Mothers with Gestational Diabetes
25. Isolated short stature as the only presenting symptom of glycogen storage disease type 0a in a Chinese child: A case report.
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