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European Journal of Medical Genetics|March 18, 2008
Direct tandem duplication in chromosome 19q characterized by array CGHMaria Palomares Bralo, Alicia Delicado, Pablo Lapunzina, et al.
Cell Transplantation|August 20, 2010
A neuroregenerative human ensheathing glia cell line with conditional rapid growthVega García-Escudero, Ricardo Gargini, María Teresa Gallego-Hernández, et al.
BMC Medical Genetics|November 1, 2014
Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrierAlicia Delicado, Luis Fernández, María Luisa de Torres, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
Craniofacial dyssynostosis: description of the first four Spanish cases and reviewEva Bermejo, Valentín Félix, Pablo Lapunzina, et al.
BMC Medical Genetics|June 4, 2009
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and reviewLuis Fernández, Julián Nevado, Fernando Santos, et al.
American Journal of Human Genetics|March 2, 2010
Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLSFeng Zhang, Lorraine Potocki, Jacinda B Sampson, et al.
American Journal of Medical Genetics. Part A|April 4, 2008
Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletionLuis Fernández, Pablo Lapunzina, Isidora López Pajares, et al.
American Journal of Medical Genetics. Part A|June 27, 2013
Customized high resolution CGH-array for clinical diagnosis reveals additional genomic imbalances in previous well-defined pathological samplesElena Vallespín, María Palomares Bralo, M Ángeles Mori, et al.
American Journal of Medical Genetics. Part A|February 26, 2015
Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterizationFe Amalia García-Santiago, Víctor Martínez-Glez, Fernando Santos, et al.
American Journal of Human Genetics|August 2, 2011
Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotypeMaría Palomares, Alicia Delicado, Elena Mansilla, et al.
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