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Keyword [Prader-willi syndrome]
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1. The Study Of Imprinted Genes On Expression In Human Oocytes And Preimplantation Embryos And On Molecular Diagnosis Of Imprinting Disease Prader-Willi Syndrome
2. The Molecular Basis Of Oculocutaneous Albinism Type 1 And Prader-Willi Syndrome
3. Effects Of Assisted Reproductive Technology On DNA Methylation Patterns Of SNRPN At Imprinting Control Region Of PWS/AS
4. One Case Of Prader-Willi Syndrome With Hashimoto's Thyroiditis In Clinical And Molecular Genetics Research
5. Prader-willi Syndrome (pws) By Methylation Specific Pcr (ms-pcr), The Establishment Of The Diagnosis And Clinical Manifestations Of Endocrine Disorders Discussed
6. The Study Of Clinical Phenotype, Growth Hormone Receptor (GHR) Exon 3 Polymorphism And Early Screening And Prevention Of Prader-Willi Syndrome
7. Study Of Clinical Phenotype And Molecule Diagnostics Of Prader-Willi Syndrome
8. Mechanism Of Snord115Overexpression In Snord116Knockout Mouse Model Of Prader-Willi Syndrome
9. Abnormal Response To The Anorexic Substances In Male Snord116Deletion Mouse Model For Prader-Willi Syndrome
10. Mechanism Of Hyperghrelinemia In Snord116Knockout Mouse Model Of Prader-Willi Syndrome
11. 1. Maternal Hyperuricemia Could Increase The Risk Of Fatal Low Birth Weight 2. Case Report Of Youth Prader-Willi Syndrome And Review Of Literature
12. Microdiversity Of Lactic Acid Bacteria Enriched By Dietary Intervention In The Gut Of A Child With Prader-Willi Syndrome
13. The Study Of Endocrine And Metabolic Manifestations And Sleep-disordered Breathing In Children With Prader-Willi Syndrome
14. Clinical Analysis Of 46 Cases Of Prader-Willi Syndrome
15. Four Clinical Cases Of PRADER-WILLI Syndrome
16. Clinical Observation Of Recombinant Human Growth Hormone In Early Treatment Of Prader-willi Syndrome
17. Two Case Reports With Prader-willi Syndrome And One Case Report With 15q11-13 Duplication Syndrome
18. Effect Observation On Growth-Promoting And Influence On Related Indexes Of Replacement Therapy With Recombinant Human Growth Hormone In Children With Prader-Willi Syndrome In Shanxi Province
19. Diagnostic Algorithm Of Neonates With Prader-Willi Syndrome
20. Clinical Characteristics Analysis Of 60 Children With Prader-Willi Syndrome
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