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PubMed for id: 3660662
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Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
Cytogenet Cell Genet. 1998;81(3-4):247-53. doi: 10.1159/000015039.
Cytogenet Cell Genet. 1998.
PMID: 9730612
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.
Buiting K, Greger V, Brownstein BH, Mohr RM, Voiculescu I, Winterpacht A, Zabel B, Horsthemke B.
Buiting K, et al.
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5457-61. doi: 10.1073/pnas.89.12.5457.
Proc Natl Acad Sci U S A. 1992.
PMID: 1608955
Free PMC article.
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