Clinical Dysmorphology : Impact Factor & More
eISSN: 1473-5717pISSN: 0962-8827
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Key Metrics
CiteScore 
2.1
Impact Factor
< 5
SJR
Q2Medicine (all)
SNIP
0.44
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Topics Covered on Clinical Dysmorphology
Clinical Dysmorphology Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
SJR
| Overview | |
| Publisher | LIPPINCOTT WILLIAMS & WILKINS |
| Language | English |
| Frequency | Quarterly |
| General Details | |
| Language | English |
| Frequency | Quarterly |
| Publication Start Year | 1992 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Clinical Dysmorphology
Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.
- 6 May 2026
- Clinical dysmorphology
A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu-Cheney syndrome.
- 5 May 2026
- Clinical dysmorphology
A rare RASopathy: Noonan syndrome-like disorder with loose anagen hair caused by a protein phosphatase 1 catalytic subunit beta pathogenic variant.
- 28 Apr 2026
- Clinical dysmorphology
Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder.
- 1 Apr 2026
- Clinical dysmorphology
Craniosynostosis in craniometaphyseal dysplasia: an expansion of phenotype.
- 23 Mar 2026
- Clinical dysmorphology
Binder phenotype with palatal epulis in a girl with chromosome 5 duplication.
- 13 Mar 2026
- Clinical dysmorphology
Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases.
- 6 May 2026
- Clinical dysmorphology
A case of serpentine fibula-polycystic kidney syndrome presenting with foetal limb shortening: a disorder of foetal osteogenesis and part of the phenotypic spectrum of Hajdu-Cheney syndrome.
- 5 May 2026
- Clinical dysmorphology
A rare RASopathy: Noonan syndrome-like disorder with loose anagen hair caused by a protein phosphatase 1 catalytic subunit beta pathogenic variant.
- 28 Apr 2026
- Clinical dysmorphology
Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder.
- 1 Apr 2026
- Clinical dysmorphology
Craniosynostosis in craniometaphyseal dysplasia: an expansion of phenotype.
- 23 Mar 2026
- Clinical dysmorphology
Binder phenotype with palatal epulis in a girl with chromosome 5 duplication.
- 13 Mar 2026
- Clinical dysmorphology
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