Research map: Target MECP2 and FMR1 Genes in Children with Global Developmental Delay

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Papers in this map

  1. A Novel FMR1 PCR Method for the Routine Detection of Low Abundance Expanded Alleles and Full Mutations in Fragile X Syndrome · Stela Filipovic-Sadic · 2010 · 283 citations · Cited by this paper
  2. Potential Role of Omega-3 Supplementation in Modulating Symptoms and Holter Parameters in Pediatric Inappropriate Sinus Tachycardia · Mohamed A. EL- Baz · 2026 · 1 citation · Related
  3. Rett syndrome · Wendy Anne Gold · 2024 · 71 citations · Cited by this paper
  4. Seizures Unmasking Bilateral Pulmonary Arteriovenous Malformations in a Child with Hereditary Hemorrhagic Telangiectasia · 2026 · Related
  5. Comprehensive evaluation of the child with global developmental delays or intellectual disability · Abdullah Nasser Aldosari · 2024 · 25 citations · Cited by this paper
  6. Regional DTI Metrics as Predictor of Early Developmental Outcome in Term Neonates with HIE · 2026 · Related
  7. Diagnostic mutational analysis of MECP2 in Korean patients with Rett syndrome · In-Joo Kim · 2006 · 16 citations · Cited by this paper
  8. Neonatal Alexander Disease with Congenital Hydrocephalus and Brainstem Involvement · 2026 · Related
  9. A Nest for Every Preterm Newborn: Making Developmental Positioning a Reality · 2026 · Related
  10. Beyond Conventional Biomarkers: Exploring Soluble Programmed Death Ligand-1 (sPD-L1) in Neonatal Sepsis · 2026 · Related
  11. Infantile Takayasu Arteritis Mimicking Kawasaki Disease in a 3-Month-Old Infant · 2026 · Related
  12. Point-of-Care Echocardiography in Pediatric and Neonatal Care · 2026 · Related
  13. Fever-Triggered Recurrent Acute Liver Failure Due to NBAS Mutation in a Child · 2026 · Related
  14. Clustered Mumps Cases at a Tertiary Care Centre in New Delhi, India · 2026 · Related

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