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Keyword [Prader-willi syndrome]
Result: 21 - 31 | Page: 2 of 2
21. Clinical Analysis Of 7 Cases Of Prader-Willi Syndrome
22. Role of the Prader-Willi syndrome proteins necdin and Magel2 in the nervous system
23. The molecular control of zebrafish isotocin cell development: A potential model for the neurodevelopmental causes of autism and Prader -Willi syndrome
24. Investigation of the Prader-Willi syndrome protein MAGEL2 in the regulation of Forkhead box transcription factor FOXO1
25. The Magel2-null mouse as a model of Prader-Willi Syndrome
26. Neural mechanisms underlying hyperphagia in Prader-Willi syndrome: An fMRI investigation
27. Elucidation of imprinting mechanisms and phenotypes in Prader-Willi syndrome mice
28. The use of sandplay therapy, the therapeutic relationship and the use of cognitive restructuring for the treatment of Prader-Willi syndrome: Case study
29. Diverse mechanisms of human genetic disease: Splice order determination in the COL1A2 gene. Effects that influence splice site mutations in osteogenesis imperfecta and a translocation disrupting SNRPN gene causes Prader-Willi syndrome
30. The Relationship Between Caring for Individuals Diagnosed with Prader-Willi Syndrome and Caregiver Stres
31. Clinical Features Of Prader-Willi Syndrome In Infancy And Follow-up Of Early Application Of Growth Hormone
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