Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Prader-Willi Syndrome and MAGEL2[original query] |
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| MAGEL2-related disorders: A study and case series. Clinical genetics 2019 8 96 (6): 493-505. Patak Jameson, Gilfert James, Byler Melissa, Neerukonda Vamsee, Thiffault Isabelle, Cross Laura, Amudhavalli Shivarajan, Pacio-Miguez Marta, Palomares-Bralo Maria, Garcia-Minaur Sixto, Santos-Simarro Fernando, Powis Zoe, Alcaraz Wendy, Tang Sha, Jurgens Julie, Barry Brenda, England Eleina, Engle Elizabeth, Hess Jonathon, Lebel Robert |
| Polysomnographic characteristics and sleep-disordered breathing in Schaaf-Yang syndrome. Pediatric pulmonology 2020 9 55 (11): 3162-3167. Powell Weston T, Schaaf Christian P, Rech Megan E, Wrede Joan |
| Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome. The Journal of clinical endocrinology and metabolism 2020 6 105 (8): 2732-9. Meader Brooke N, Albano Alessandro, Sekizkardes Hilal, Delaney Ange |
| Loss-of-function G6PD variant moderated high fat diet-induced obesity, adipocyte hypertrophy, and fatty liver in male rats. The Journal of biological chemistry 2024 6 107460. Shun Matsumura, Christina Signoretti, Samuel Fatehi, Bat Ider Tumenbayar, Catherine D'Addario, Erik Nimmer, Colin Thomas, Trisha Viswanathan, Alexandra Wolf, Victor Garcia, Petra Rocic, Yongho Bae, S M Shafiqul Alam, Sachin A Gup |
- Page last reviewed:Feb 1, 2024
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