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L Pasquier

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 16, 2011

Binder phenotype in mothers affected with autoimmune disordersE Colin, R Touraine, J M Levaillant, et al.

Journal of Medical Genetics|September 25, 2008

2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.

Clinical Genetics|May 29, 2010

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patientsA M Alazami, S A Schneider, D Bonneau, et al.

Archives of Disease in Childhood|January 24, 2006

Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.

Physical Chemistry Chemical Physics : PCCP|March 11, 2022

Two-dimensional square and hexagonal oxide quasicrystal approximants in SrTiO3 films grown on Pt(111)/Al2O3(0001)C Ruano Merchan, T T Dorini, F Brix, et al.

Journal of Medical Genetics|October 4, 2005

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.

Small (Weinheim an Der Bergstrasse, Germany)|September 19, 2025