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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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