Romulus C. Grigorescu
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
First reports of fetal SMARCC1 related hydrocephalus.
Journal: European journal of medical genetics
Published: November 27, 2022
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Journal: Journal of medical genetics
Published: November 16, 2020
Merged bilateral arterial duct and circumflex retroesophageal right aortic arch in a fetus with normal intracardiac anatomy.
Journal: Cardiology in the young
Published: November 05, 2019
Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly.
Journal: Clinical genetics
Published: April 05, 2017
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis.
Journal: American journal of human genetics
Published: June 03, 2016
AIRP best cases in radiologic-pathologic correlation: prenatal and postmortem imaging of a complex cloacal malformation.
Journal: Radiographics : a review publication of the Radiological Society of North America, Inc
Published: November 11, 2014
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
Journal: Orphanet journal of rare diseases
Published: March 27, 2013
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome.
Journal: European journal of medical genetics
Published: November 06, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026