Publications by authors named "Romulus Grigorescu"

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First reports of fetal SMARCC1 related hydrocephalus.
Nicolas Rive Le Gouard, Romain Nicolle, Mathilde Lefebvre, Antoinette Gelot, Solveig Heide, Romulus Grigorescu

Eur J Med Genet· August 2023

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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, Jérome Maluenda, Dan Mejlachowicz, Romulus Grigorescu

J Med Genet· June 2022

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Merged bilateral arterial duct and circumflex retroesophageal right aortic arch in a fetus with normal intracardiac anatomy.
Saïd Bichali, Romulus Cristian Grigorescu, Mathilde Lefebvre, Charlotte Oriot, Ferdinand Dhombres

Cardiol Young· December 2019

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Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis.
Jérôme Maluenda, Constance Manso, Loic Quevarec, Alexandre Vivanti, Florent Marguet, Romulus Grigorescu

Am J Hum Genet· October 2016

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AIRP best cases in radiologic-pathologic correlation: prenatal and postmortem imaging of a complex cloacal malformation.
Cindy Fayard, Eléonore Blondiaux, Romulus Grigorescu, Catherine Garel

Radiographics· November 2015

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Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
Bruno Donadille, Pascal D'Anella, Martine Auclair, Nancy Uhrhammer, Marc Sorel, Romulus Grigorescu

Orphanet J Rare Dis· July 2013

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Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome.
Chloé Quélin, Philippe Loget, Alain Verloes, Anne Bazin, Bettina Bessières, Romulus Grigorescu

Eur J Med Genet· February 2012

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