M. Carmen Valero

A Highly Sensitive Genetic Protocol to Detect NF1 Mutations

M. Carmen Valero, Yolanda Martín, Elisabete Hernández-Imaz et al. · Journal of Molecular Diagnostics · 2011 · 117 citations · Full text

Detect Nf1 Mutations, Genetic Analysis, Genetic Testing +6

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)

M. Carmen Valero, Oscar de Luis, Jesús Cruces et al. · Genomics · 2000 · 107 citations

Human 7Q11.23, Fine-scale Comparative Mapping, Genetics +9

Eccentric Exercise Facilitates Mesenchymal Stem Cell Appearance in Skeletal Muscle

M. Carmen Valero, Heather D. Huntsman, Jianming Liu et al. · PLoS ONE · 2012 · 87 citations · Full text

WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog

Oscar de Luis, M. Carmen Valero, L.A. Pérez Jurado · European Journal of Human Genetics · 2000 · 66 citations · Full text

Transcriptional Regulation, Developmental Biology, Complete Characterisation +12

Identification of de novo deletions at the NF1 gene: no preferential paternal origin and phenotypic analysis of patients

M. Carmen Valero, I Pascual-Castroviejo, Eladio A. Velasco et al. · Human Genetics · 1997 · 49 citations

Phenotypic Analysis, Mendelian Disorder, Genetic Disorder +8