Clinical Dysmorphology
Published by Wolters Kluwer Health
ISSN : 0962-8827 eISSN : 1473-5717
Abbreviation : Clin. Dysmorphol.
Aims & Scope
Clinical Dysmorphology publishes succinct case reports on the etiology, clinical delineation, genetic mapping, and molecular embryology of birth defects.
This journal covers such topics as multiple congenital anomaly syndromes - with particular emphasis on previously undescribed conditions, rare findings, ethnic differences in existing syndromes, fetal abnormalities, and cytogenetic aberrations that might give clues to the localization of developmental genes.
Regular features include original, peer-reviewed articles, conference reports, book and software reviews, abstracts and summaries from the UK Dysmorphology Club, and literature summaries.
Submitted articles undergo a preliminary review by the editor.
Some articles may be returned to authors wihtout further consideration.
Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
View Aims & ScopeMetrics & Ranking
Impact Factor
Year | Value |
---|---|
2025 | 0.5 |
2024 | 0.40 |
Journal Rank
Year | Value |
---|---|
2024 | 17952 |
Journal Citation Indicator
Year | Value |
---|---|
2024 | 80 |
SJR (SCImago Journal Rank)
Year | Value |
---|---|
2024 | 0.265 |
Quartile
Year | Value |
---|---|
2024 | Q3 |
h-index
Year | Value |
---|---|
2024 | 33 |
Impact Factor Trend
Abstracting & Indexing
Journal is indexed in leading academic databases, ensuring global visibility and accessibility of our peer-reviewed research.
Subjects & Keywords
Journal’s research areas, covering key disciplines and specialized sub-topics in Medicine, designed to support cutting-edge academic discovery.
Most Cited Articles
The Most Cited Articles section features the journal's most impactful research, based on citation counts. These articles have been referenced frequently by other researchers, indicating their significant contribution to their respective fields.
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Macrocephaly with cutis marmorata, haemangioma and syndactyly ??? a distinctive overgrowth syndrome
Citation: 108
Authors: J, B, H, L, A, R C M, R F, L, M, J, D
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Kabuki syndrome: a review study of three hundred patients
Citation: 96
Authors: Marja W., Alice S., Jeannette, Martinus F., Patrick J.
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Kabuki make-up (Niikawa-Kuroki) syndrome
Citation: 85
Authors: N., P., A., J., S., R., E., D., A., D., M., H., I., A., M., G.
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Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)
Citation: 81
Authors: Jeanne, Peter M., Mayada, Andrew P., Robin M.
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Chondrodysplasia punctata: a clinical diagnostic and radiological review
Citation: 79
Authors: Melita D., Lyn S., Sahar, Christine M.
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A family with autosomal dominant oculo-auriculo-vertebral spectrum
Citation: 68
Authors: Christiane, Frank, Stefan, Sven, Hermann-Josef, Gabriele, Dagmar