These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
27. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence. Lukusa T; Fryns JP Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663 [TBL] [Abstract][Full Text] [Related]
28. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings. Angulo MA; Butler MG; Cataletto ME J Endocrinol Invest; 2015 Dec; 38(12):1249-63. PubMed ID: 26062517 [TBL] [Abstract][Full Text] [Related]
29. Structural Models for the Dynamic Effects of Loss-of-Function Variants in the Human SIM1 Protein Transcriptional Activation Domain. Coban MA; Blackburn PR; Whitelaw ML; Haelst MMV; Atwal PS; Caulfield TR Biomolecules; 2020 Sep; 10(9):. PubMed ID: 32932609 [TBL] [Abstract][Full Text] [Related]
30. Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region. Chrast R; Scott HS; Chen H; Kudoh J; Rossier C; Minoshima S; Wang Y; Shimizu N; Antonarakis SE Genome Res; 1997 Jun; 7(6):615-24. PubMed ID: 9199934 [TBL] [Abstract][Full Text] [Related]
31. First Case Report of Prader-Willi-Like Syndrome in Colombia. Candelo E; Feinstein MM; Ramirez-Montaño D; Gomez JF; Pachajoa H Front Genet; 2018; 9():98. PubMed ID: 29619043 [No Abstract] [Full Text] [Related]
32. [Prader-Willi syndrome associated with chromosomal aberration: report of a case]. Kokura K; Shima H; Mori Y; Ikoma F; Sakamoto H; Furuyama J Hinyokika Kiyo; 1992 Sep; 38(9):1079-82. PubMed ID: 1357945 [TBL] [Abstract][Full Text] [Related]