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Topics Covered on CONGENITAL ANOMALIES
CONGENITAL ANOMALIES Journal Specifications
Indexed in the following public directories
Web of Science
| Overview | |
| Publisher | WILEY |
| Language | English |
| Frequency | Quarterly |
| General Details | |
| Language | English |
| Frequency | Quarterly |
| Publication Start Year | 1960 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in CONGENITAL ANOMALIES
Clinical and Genetic Findings in Two Japanese Individuals With SET-Related Neurodevelopmental Disorder.
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Hypoplastic Left Heart Syndrome Variant With Unexpected Early Sudden Death in a Newborn Infant With ZTTK Syndrome.
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Congenital Anomalies and Consanguinity in a Rural Community of Punjab, Pakistan: A Cross-Sectional Study.
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Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia-Gibbs Syndrome.
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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
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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