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CONGENITAL ANOMALIES : Impact Factor & More

eISSN: 1741-4520pISSN: 0914-3505

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CONGENITAL ANOMALIES Journal Specifications

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Overview
Publisher WILEY
Language English
Frequency Quarterly
General Details
LanguageEnglish
FrequencyQuarterly
Publication Start Year1960
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in CONGENITAL ANOMALIES

Clinical and Genetic Findings in Two Japanese Individuals With SET-Related Neurodevelopmental Disorder.
  • 1 Feb 2026
  • Congenital anomalies
Hypoplastic Left Heart Syndrome Variant With Unexpected Early Sudden Death in a Newborn Infant With ZTTK Syndrome.
  • 1 Feb 2026
  • Congenital anomalies
Congenital Anomalies and Consanguinity in a Rural Community of Punjab, Pakistan: A Cross-Sectional Study.
  • 1 Feb 2026
  • Congenital anomalies
Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia-Gibbs Syndrome.
  • 1 Feb 2026
  • Congenital anomalies
Aberrant Splicing From an HDAC8 Intronic Variant c.112-15C>A Causes Familial Cornelia de Lange Syndrome in Heterozygous and Hemizygous Individuals.
  • 1 Feb 2026
  • Congenital anomalies
Mosaic Variant in Unilateral Woolly Hair in a Girl With PIK3CA-Related Overgrowth Spectrum.
  • 1 Feb 2026
  • Congenital anomalies
Clinical and Genetic Findings in Two Japanese Individuals With SET-Related Neurodevelopmental Disorder.
  • 1 Feb 2026
  • Congenital anomalies
Hypoplastic Left Heart Syndrome Variant With Unexpected Early Sudden Death in a Newborn Infant With ZTTK Syndrome.
  • 1 Feb 2026
  • Congenital anomalies
Congenital Anomalies and Consanguinity in a Rural Community of Punjab, Pakistan: A Cross-Sectional Study.
  • 1 Feb 2026
  • Congenital anomalies
Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia-Gibbs Syndrome.
  • 1 Feb 2026
  • Congenital anomalies
Aberrant Splicing From an HDAC8 Intronic Variant c.112-15C>A Causes Familial Cornelia de Lange Syndrome in Heterozygous and Hemizygous Individuals.
  • 1 Feb 2026
  • Congenital anomalies
Mosaic Variant in Unilateral Woolly Hair in a Girl With PIK3CA-Related Overgrowth Spectrum.
  • 1 Feb 2026
  • Congenital anomalies

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