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Inversion duplication deletions involving the long arm of chromosome 13: Phenotypic description of additional three fetuses and genotype–phenotype correlation
Authors:Chloe Quelin  Emmanuel Spaggiari  Suonavy Khung‐Savatovsky  Celine Dupont  Laurent Pasquier  Laurence Loeuillet  Sylvie Jaillard  Josette Lucas  Pascale Marcorelles  Hubert Journel  Khantaby Pluquailec‐Bilavarn  Anne Bazin  Alain Verloes  Anne‐Lise Delezoide  Azzedine Aboura  Fabien Guimiot
Affiliation:1. Department of Developmental Biology, AP‐HP, Robert Debré University Hospital, Paris and Diderot University, Paris, France;2. Clinical Genetics Unit, Rennes Sud University Hospital, Rennes, France;3. Cytogenetics Unit, AP‐HP, Robert Debré University Hospital, Paris Diderot University, Paris, France;4. Pathology Laboratory, Poissy Hospital, Saint Germain en Laye, France;5. Cytogenetics Unit, Rennes Pontchaillou University Hospital, Rennes, France;6. Pathology Laboratory, Pole Pathologie‐Biologie, Brest University Hospital, Brest, France;7. Clinical Genetics Unit, CHBA, Chubert Hospital, Vannes, France;8. Cytogenetics Laboratory, Cesson‐Sévigné, France;9. Cerba Laboratory, Cergy‐Pontoise, France;10. Department of Genetic, AP‐HP, Robert Debré University Hospital, Paris and Diderot University, Paris, France
Abstract:
Keywords:prenatal  inv dup del 13q  phenotype
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