Micromelic upper limbs and cardiac defect: A fetal case of Holt-Oram syndrome identified in the first trimester - European Journal of Obstetrics and Gynecology and Reproductive Biology
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome) | NEJM
The Holt-Oram syndrome Tbx5 proteins with mutations R237Q and R279ter... | Download Scientific Diagram
TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype | European Journal of Human Genetics
تويتر \\ Interesting MediCine 🤩🩺 على تويتر: "🛑Holt-Oram syndrome is characterized by skeletal abnormalities of the hands ✋🏻and arms upper limbs) and heart ♥️ People with Holt-Oram syndrome have abnormally developed bones
Holt-Oram Syndrome
Clinical photograph of a patient with Holt-Oram syndrome with right non... | Download Scientific Diagram
Holt-Oram Syndrome | Circulation
Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease - ScienceDirect
Cureus | Holt-Oram Syndrome: An Incidental Diagnosis
Prevalence of Holt Oram syndrome patients per 16 selected EUROCAT... | Download Table
Cureus | Holt-Oram Syndrome: An Incidental Diagnosis
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Holt-Oram Syndrome | Circulation
Holt-Oram syndrome: MedlinePlus Genetics
The human model for congenital heart disease – Developmental Biology Research Highlights, University of Otago, New Zealand
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome | Pediatric Research
Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis | Walencka | Ginekologia Polska
A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene | Semantic Scholar
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PDF) Holt Oram syndrome: a registry-based study in Europe | Ingeborg Barisic - Academia.edu
Diversity of congenital cardiac defects and skeletal deformities associated with the Holt–Oram syndrome - ScienceDirect
Holt-Oram syndrome: MedlinePlus Genetics
Different TBX5 interactions in heart and limb defined by Holt–Oram syndrome mutations | PNAS
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome) | NEJM
PDF] Holt-Oram Syndrome With Multiple Cardiac Abnormalities | Semantic Scholar
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Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome - He - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library
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Congenital superior oblique palsy in a patient with Holt-Oram syndrome | SpringerLink
Different TBX5 interactions in heart and limb defined by Holt–Oram syndrome mutations | PNAS
Atrial septal defect - Wikipedia
Genetic Heterogeneity of Heart-Hand Syndromes | Circulation
What Is Holt-Oram Syndrome? (with pictures)
SOLVED: baby born with Holt-Oram syndrome can present with defects In the development of the heart and llmbs. The heart can have an Atrial Septal Defect (A red arrow) the hands may
Holt-Oram syndrome: A case report | Revista Portuguesa de Cardiologia (English edition)
Identification and functional analysis of genetic variants in TBX5 gene promoter in patients with acute myocardial infarction | BMC Cardiovascular Disorders | Full Text
Holt-Oram syndrome: a clinical genetic study. - Abstract - Europe PMC
Frontiers | Prenatal Diagnosis of Holt–Oram Syndrome With a Novel Mutation of TBX5 Gene: A Case Report
A novel de novo TBX5 mutation in a patient with Holt–Oram s | TACG
Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis | Walencka | Ginekologia Polska
Holt-Oram syndrome leads to heart transplant - Heart Foundation
Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease - ScienceDirect
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome) | NEJM
Holt-Oram syndrome: a clinical genetic study. - Abstract - Europe PMC
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A Rare Variant and Unusual Presentation of Holt Oram Syndrome in a Child - Cureus
Tbx5 del / ϩ Mice Are a Model of Holt-Oram Syndrome | Download Scientific Diagram
Holt-Oram Syndrome With Multiple Cardiac Abnormalities | Spiridon | Cardiology Research
SciELO - Brasil - A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve A novel TBX5 mutation predisposes to familial cardiac septal
A novel de novo TBX5 mutation in a patient with Holt–Oram s | TACG
A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation | Circulation Research
Holt-Oram Syndrome | Radiology Key
Functional analysis of two novel TBX5 variants present in individuals with Holt–Oram syndrome with different clinical manifestations | SpringerLink
Holt-Oram syndrome: MedlinePlus Genetics
Holt oram syndrome presentation
PDF] Holt-Oram Syndrome With Multiple Cardiac Abnormalities | Semantic Scholar
Holt-Oram syndrome
Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants | European Journal of Human Genetics
What Is Holt-Oram Syndrome? (with pictures)
Holt‐Oram Syndrome - Sepulveda - 2004 - Journal of Ultrasound in Medicine - Wiley Online Library
Holt-Oram syndrome
SciELO - Brasil - Holt-Oram syndrome revisited. Two patients in the same family Holt-Oram syndrome revisited. Two patients in the same family
Genes | Free Full-Text | From Stem Cells to Populations—Using hiPSC, Next-Generation Sequencing, and GWAS to Explore the Genetic and Molecular Mechanisms of Congenital Heart Defects
Holt-Oram syndrome: A case report | Revista Portuguesa de Cardiologia (English edition)
Holt-Oram syndrome: a clinical geneticstudy
Holt-Oram syndrome
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Holt-Oram Syndrome With Multiple Cardiac Abnormalities | Spiridon | Cardiology Research
Holt oram syndrome presentation
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome) | NEJM
Holt Oram syndrome | Radiology Case | Radiopaedia.org
Figure 2 from A case report on holt-oram syndrome (heart-hand) | Semantic Scholar
Holt Oram Syndrome - an overview | ScienceDirect Topics
Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis | Walencka | Ginekologia Polska
Holt–Oram syndrome – Case series of two reports Ilyas M, Wani AA, Ahmad Z, Ahmad Kazimi MJ, Choh NA - CHRISMED J Health Res
Atypical Carpal Tunnel Syndrome in a Holt Oram Patient: A Case Report and Literature Review
Em>TBX5</em> variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects
Identification of a novel TBX5 c.755 + 1 G > A variant and related pathogenesis in a family with Holt–Oram syndrome - Wang - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library
Pediatric Holt-Oram Syndrome Clinical Presentation: History, Physical, Severity Scoring System
Association of TBX5 gene polymorphism with ventricular septal defect in the Chinese Han population
Frontiers | Discovering miRNA Regulatory Networks in Holt–Oram Syndrome Using a Zebrafish Model
Em>TBX5</em> variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects
JCDD | Free Full-Text | Considering the Genetic Architecture of Hypoplastic Left Heart Syndrome
Causes and Symptoms of Hypoplastic Left Heart Syndrome
▷ Celebrities with Holt Oram Syndrome
A TBX5 3′UTR variant increases the risk of congenital heart disease in the Han Chinese population | Cell Discovery