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
Application of deep learning and explainable AI-supported medical decision-making for facial phenotyping in genetic syndromes.
- 8 Oct 2026
- Clinical dysmorphology
A prenatal-onset severe phenotype of SLC35A2-related congenital disorder of glycosylation associated with a mosaic hemizygous intronic variant.
- 6 Oct 2026
- Clinical dysmorphology
Second-trimester prenatal phenotype of complete trisomy 10 with combined encephalocele and myelomeningocele.
- 29 Sep 2026
- Clinical dysmorphology
Expanding the phenotype of GDI1-related neurodevelopmental disorder: report of the fifth family.
- 29 Sep 2026
- Clinical dysmorphology
Marbach-Rustad progeroid syndrome caused by a hotspot LEMD2 variant: expanding the phenotypic spectrum with skeletal, cutaneous, and renal findings.
- 23 Sep 2026
- Clinical dysmorphology
Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant.
- 14 Sep 2026
- Clinical dysmorphology
Application of deep learning and explainable AI-supported medical decision-making for facial phenotyping in genetic syndromes.
- 8 Oct 2026
- Clinical dysmorphology
A prenatal-onset severe phenotype of SLC35A2-related congenital disorder of glycosylation associated with a mosaic hemizygous intronic variant.
- 6 Oct 2026
- Clinical dysmorphology
Second-trimester prenatal phenotype of complete trisomy 10 with combined encephalocele and myelomeningocele.
- 29 Sep 2026
- Clinical dysmorphology
Expanding the phenotype of GDI1-related neurodevelopmental disorder: report of the fifth family.
- 29 Sep 2026
- Clinical dysmorphology
Marbach-Rustad progeroid syndrome caused by a hotspot LEMD2 variant: expanding the phenotypic spectrum with skeletal, cutaneous, and renal findings.
- 23 Sep 2026
- Clinical dysmorphology
Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant.
- 14 Sep 2026
- Clinical dysmorphology
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