Patient with Helsmoortel-van der Aa Syndrome and O'Donnell-Luria-Rodan Syndrome: a case report | Brazilian Journal of Case Reports
Whole Exome Sequencing Leads to Helsmoortel-van der Aa Syndrome Diagnosis - Global Genes
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IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome
Early behavioral and developmental interventions in ADNP‐syndrome: A case report of SWI/SNF‐related neurodevelopmental syndrome - Shillington - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
ADNP (Helsmoortel-van der AA Syndrome) Awareness – Littlest Warrior
Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement - ScienceDirect
Helsmoortel-van der Aa syndrome Archives – Shopaholic and Babies
Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report
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Clinical impact and in vitro characterization of ADNP variants in pediatric patients | Molecular Autism | Full Text
IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome
IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome
ADNP syndrome: MedlinePlus Genetics
Helsmoortel-van der Aa syndrome Archives – Shopaholic and Babies
A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome | European Journal of Human Genetics
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Helsmoortel-van der Aa Syndrome: What Late Development Meant for Hanna - Global Genes
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Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation | Journal of Molecular Neuroscience
Frontiers | The ADNP Syndrome and CP201 (NAP) Potential and Hope
Helsmoortel-Van Der Aa Syndrome | Signs, Symptoms, Support
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