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Publications by Aurélie Mezel
Holt-Oram Syndrome: Clinical and Molecular Description of 78 Patients With TBX5 Variants
European Journal of Human Genetics
Genetics
Related publications
EP13.08: Prenatal Diagnosis of Holt-Oram Syndrome
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
The Syndrome of Familial Defects of Heart and Upper Extremities (Holt-Oram Syndrome)
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Holt-Oram Syndrome in Two Families Diagnosed With Left Ventricular Non-Compaction and Conduction Disease
HeartRhythm Case Reports
Cardiovascular Medicine
Cardiology
Syndromic Anorectal Malformation Associated With Holt–Oram Syndrome, Microcephaly, and Bilateral Corneal Opacity: A Case Report
Journal of Medical Case Reports
Medicine
Possible Holt-Oram Syndrome: Missed Prenatal Diagnosis and Sub-Optimal Management in a Poor-Resourced Hospital
Balkan Medical Journal
Medicine
Síndrome De Holt-Oram: (Presentación De Dos Casos Clínicos)
Revista Chilena de Pediatria
Child Health
Pediatrics
Perinatology
Atrial Septal Defect Type II and Upper Limb Malformation in 40-Year-Old Male as a Manifestation of Holt-Oram Syndrome
Cardiology Journal
Medicine
Cardiovascular Medicine
Cardiology
Clinical, Immunological and Molecular-Genetic Description of Symptoms in Children With Autoimmune Polyglandular Syndrome Type 1: Description of a Case Series
Voprosy Sovremennoi Pediatrii - Current Pediatrics
Child Health
Pediatrics
Perinatology
A Novel Mutated Sequence in the T-Box Transcription Factor-5 (TBX-5) Gene (C.241A>T) in Holt–Oram Syndrome
Journal of the Turkish German Gynecology Association
Gynecology
Obstetrics
