Valero, M.C.; de Luis, O.; Cruces, J.; Pérez Jurado, L.A. "Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).". Genomics. 69(1): 1-13. (2000). (PMID: 11013070).
Pérez Jurado, L.A.; Wang, Y.K.; Francke, U.; Cruces, J. "TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog.". Cytogenet. Cell Genet.. 86(3-4): 277-284. (1999). (PMID: 10575226).
de la Puente, A.; Velasco, E.; Pérez Jurado, L.A.; Hernández-Chico, C.; van de Rijke, F.M.; Scherer, S.W.; Raap, A.K.; Cruces, J. "Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7.". Cytogenet. Cell Genet.. 83(3-4): 176-181. (1998). (PMID: 10072574).
Pérez Jurado, L.A.; Wang, Y.K.; Peoples, R.; Coloma, A.; Cruces, J.; Francke, U. "A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK.". Hum. Mol. Genet.. 7(3): 325-334. (1998). (PMID: 9466987).
Instituto de Investigaciones Biomédicas "Alberto Sols"
C/Arturo Duperier 4. 28029 Madrid. (Spain)
Tel +(34) 91 585 4400 // Fax +(34) 91 558 4401 Email:Info
Email:Info