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Oncotarget|August 4, 2016
Telomere status in chronic lymphocytic leukemia with TP53 disruptionRomain Guièze, Mélanie Pages, Lauren Véronèse, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|June 28, 2016
A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardationCarole Goumy, Mathilde Gay-Bellile, Gaelle Salaun, et al.Oncotarget|November 5, 2017
TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancerMathilde Gay-Bellile, Lauren Véronèse, Patricia Combes, et al.Andrology|August 26, 2022
Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short statureCéline Capron, Louis Januel, Gaëlle Vieville, et al.Prenatal Diagnosis|March 29, 2016
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyNicolas Gruchy, Eleonore Blondeel, Nathalie Le Meur, et al.Prenatal Diagnosis|May 13, 2015
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnanciesFrancesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, et al.Prenatal Diagnosis|July 6, 2019
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?Kamran Moradkhani, Laurence Cuisset, Pierre Boisseau, et al.Journal of Medical Genetics|October 6, 2018
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlationsLaïla Allach El Khattabi, Solveig Heide, Jean-Hubert Caberg, et al.NPJ Genomic Medicine|July 10, 2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.NPJ Genomic Medicine|December 22, 2017
A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.Pageof 4