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Clinical Dysmorphology : Impact Factor & More

eISSN: 1473-5717pISSN: 0962-8827

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 Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher LIPPINCOTT WILLIAMS & WILKINS
Language English
Frequency Quarterly
General Details
LanguageEnglish
FrequencyQuarterly
Publication Start Year1992
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Clinical Dysmorphology

Generalized overgrowth in CDC42BPB-related Chilton-Okur-Chung neurodevelopmental syndrome: expanding the phenotypic spectrum.
  • 20 Jul 2026
  • Clinical dysmorphology
Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.
  • 20 Jul 2026
  • Clinical dysmorphology
Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion.
  • 17 Jul 2026
  • Clinical dysmorphology
Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.
  • 1 Jul 2026
  • Clinical dysmorphology
Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features.
  • 1 Jul 2026
  • Clinical dysmorphology
Endocrine-predominant type 2 Woodhouse-Sakati syndrome caused by a novel homozygous DCAF17 variant.
  • 1 Jul 2026
  • Clinical dysmorphology
Generalized overgrowth in CDC42BPB-related Chilton-Okur-Chung neurodevelopmental syndrome: expanding the phenotypic spectrum.
  • 20 Jul 2026
  • Clinical dysmorphology
Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.
  • 20 Jul 2026
  • Clinical dysmorphology
Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion.
  • 17 Jul 2026
  • Clinical dysmorphology
Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.
  • 1 Jul 2026
  • Clinical dysmorphology
Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features.
  • 1 Jul 2026
  • Clinical dysmorphology
Endocrine-predominant type 2 Woodhouse-Sakati syndrome caused by a novel homozygous DCAF17 variant.
  • 1 Jul 2026
  • Clinical dysmorphology

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