BioMed Central | Articles which cite: Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.

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PubMed Central articles that cite the above article:

1.	SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U PLoS ONE 2008, 3:e1709 [PubMed Central] [PubMed] [Related articles]
2.	Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. Skryabin BV, Gubar LV, Seeger B, Pfeiffer J, Handel S, Robeck T, Karpova E, Rozhdestvensky TS, Brosius J PLoS Genet 2007 Dec 28, 3:e235 [PubMed Central] [PubMed] [Related articles]

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