Kamran Moradkhani

Years Active: 2019-2019
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Kamran Moradkhani, Laurence Cuisset, Pierre Boisseau, Olivier Pichon, Marine Lebrun, Houda Hamdi-Rozé, Marie-Laure Maurin, Nicolas Gruchy, Marie-Christine Manca-Pellissier, Perrine Malzac, Frédéric Bilan, Marie-Pierre Audrezet, Pascale Saugier-Veber, Anne-Laure Fauret-Amsellem, Chantal Missirian, Paul Kuentz, Gregory Egea, Agnès Guichet, Isabelle Creveaux, Caroline Janel, Ines Harzallah, Renaud Touraine, Carole Goumy, Nicole Joyé, Jacques Puechberty, Emmanuelle Haquet, Sandra Chantot-Bastaraud, Sébastien Schmitt, Philippe Gosset, Bénédicte Duban-Bedu, Bruno Delobel, Philippe Vago, François Vialard, Denise Molina Gomes, Jean-Pierre Siffroi, Jean-Paul Bonnefont, Jean-Michel Dupont, Philippe Jonveaux, Martine Doco-Fenzy, Damien Sanlaville, Cédric Le Caignec
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? Prenatal diagnosis 39 (11) (2019)
Sarah Guterman, Claire Beneteau, Sylvia Redon, Céline Dupont, Chantal Missirian, Pauline Jaeger, Berenice Herve, Clémence Jacquin, Nathalie Douet-Guilbert, Marianne Till, Anne-Claude Tabet, Kamran Moradkhani, Valérie Malan, Martine Doco-Fenzy, François Vialard
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review. Prenatal diagnosis 39 (10) (2019)

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