机译:Myhre和Laps综合征:32例患者的临床和分子综述
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
Neuropediatry Department Centre de Référence Maladies Rares 'Anomalies du Développement Armand;
Department of Clinical Genetics Ersamus MCRotterdam Netherlands;
Department of Molecular and Human Genetics Baylor College of MedicineHouston TX United States;
Department of Human Genetics Institute of Pathology and GeneticsGosselies Belgium;
Unit of Rare Diseases Department of Pediatrics Gaslini InstituteGenoa Italy;
Manchester Academic Health Science Centre Genetic Medicine-University of Manchester St Mary's;
Department of Pediatrics Academic Medical Center University of AmsterdamAmsterdam Netherlands;
Genetics and Cytogenetics Department GRC-upmc Pitié-Salpétrière CHUParis France;
Department of Genetics CHUVVaud Switzerland;
Division of Clinical and Metabolic Genetics Hospital for Sick ChildrenToronto ON Canada;
Medical Genetics Massachussets General Hospital for ChildrenBoston MA United States;
Department of Clinical Genetics University HospitalLille France;
Clinical Genetics St George's Healthcare NHS TrustLondon United Kingdom;
Genetic and Medical Embryology Unit Centre de Référence des Surdités Génétiques Armand-Trousseau;
West of Scotland Regional Genetics ServiceGlasgow United Kingdom;
Manchester Academic Health Science Centre Genetic Medicine-University of Manchester St Mary's;
Institute of Human Genetics Meir Medical CenterKfar Saba Israel;
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
Department of Clinical Genetics Ersamus MCRotterdam Netherlands;
Department of Genetics University Medical Center Groningen University of GroningenGroningen;
Department of Pathology Massachussets General HospitalBoston MA United States;
Center for Human Genetics Cliniques Universitaires St-LucBrussels Belgium;
West of Scotland Regional Genetics ServiceGlasgow United Kingdom;
Department of Clinical Genetics Saint-Etienne CHUSaint-Etienne France;
Department of Medical Genetics University and University Hospital AntwerpEdegem Belgium;
Department of Medical Genetics University and University Hospital AntwerpEdegem Belgium;
Department of Genetics University Medical Center Groningen University of GroningenGroningen;
Department of Genetics INSERM U676 Robert Debré HospitalParis France;
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
Department of Genetics Paris Descartes University-Sorbonne Paris Cité Necker Enfants-Malades;
LAPS; long-term follow-up; Myhre syndrome; SMAD4;
机译:Myhre和LAPS综合征:32例患者的临床和分子检查
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机译:Myhre和LAPS综合征:32例患者的临床和分子检查
机译:Myhre和LAPS综合征:32例患者的临床和分子检查(第22卷,第1272页,2014年)