Prader-Willi syndrome: Current understanding of cause and diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference141 articles.
1. Pathology of muscular hypotonia in the Prader-Willi syndrome
2. Systematic analysis of 95 reciprocal translocations of autosomes
3. Chromosome 15 in floppy infants
4. The Prader-Willi Syndrome Regulation of Fat Transport
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1. Early psychomotor development and growth hormone therapy in children with Prader-Willi syndrome: a review;European Journal of Pediatrics;2023-11-21
2. Understanding Prader-Will Syndrome;Handbook of Research on Shifting Paradigms of Disabilities in the Schooling System;2023-10-16
3. Hormonal Imbalances in Prader–Willi and Schaaf–Yang Syndromes Imply the Evolution of Specific Regulation of Hypothalamic Neuroendocrine Function in Mammals;International Journal of Molecular Sciences;2023-08-23
4. The interaction between the nervous system and the stomatognathic system: from development to diseases;International Journal of Oral Science;2023-08-15
5. Using sno- lncRNAs as potential markers for Prader-Willi syndrome diagnosis;RNA Biology;2023-07-05
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