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Molecular characterization of 39 <i>de novo</i><scp>sSMC</scp>: contribution to prognosis and genetic counselling, a prospective studyNathalie Marle, Patrick Callier, Danielle Martinet et al.|Clinical Genetics|2013Cited by 26
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, Cédric Le Caignec, Grégory Egea et al.|Prenatal Diagnosis|2019Cited by 17
Evidence for high breakpoint variability in 46, XX, SRY‐positive testicular disorder and frequent ARSE deletion that may be associated with short statureCéline Capron, François Vialard, Louis Januel et al.|Andrology|2022Cited by 10