Publications by authors named "Stephane Serero"

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Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin.
Pascale Kleinfinger, Armelle Luscan, Léa Descourvieres, Daniela Buzas, Aicha Boughalem, Stéphane Serero

Genes (Basel)· November 2022

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Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case.
Antoine Laudat, Stéphane Serero, Isma Seridi, Laurence Burc-Struxiano

Ann Biol Clin (Paris)· December 2017

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Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
Andrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Stéphane Serero

Am J Med Genet A· October 2012

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Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.
Morgane Valentin, Annick Ottenwalter, Stéphane Serero, Françoise Muller, Dominique Luton

Prenat Diagn· December 2009

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Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.
Valérie Bélien, Marion Gérard-Blanluet, Stéphane Serero, Nathalie Le Dû, Clarisse Baumann

Am J Med Genet A· July 2008

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Isolated fetal hyperechogenic bowel associated with intra-uterine parvovirus B19 infection.
Jean-Marie Jouannic, Laurent Gavard, Joël Créquat, Françoise Muller, Stéphane Serero

Fetal Diagn Ther· January 2006

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