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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

Rafiq syndrome in a Saudi patient: novel homozygous MAN1B1 variant (c.1118C>G; p.Pro373Arg) and expanded phenotypic spectrum.
  • 18 Nov 2025
  • Clinical dysmorphology
Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overview.
  • 12 Nov 2025
  • Clinical dysmorphology
Pediatric epilepsy: a dual diagnosis of SCMARCA2-Nicolaides-Baraitser syndrome and CHRNB2-nocturnal-frontal-lobe epilepsy.
  • 25 Sep 2025
  • Clinical dysmorphology
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic review.
  • 25 Sep 2025
  • Clinical dysmorphology
Recurrent herpes labialis in a patient with interferon regulatory factor 3 deletion: a novel case report.
  • 22 Sep 2025
  • Clinical dysmorphology
Observed total and live birth prevalence of Wolf-Hirschhorn syndrome in England 2015-2020.
  • 19 Sep 2025
  • Clinical dysmorphology
Rafiq syndrome in a Saudi patient: novel homozygous MAN1B1 variant (c.1118C>G; p.Pro373Arg) and expanded phenotypic spectrum.
  • 18 Nov 2025
  • Clinical dysmorphology
Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overview.
  • 12 Nov 2025
  • Clinical dysmorphology
Pediatric epilepsy: a dual diagnosis of SCMARCA2-Nicolaides-Baraitser syndrome and CHRNB2-nocturnal-frontal-lobe epilepsy.
  • 25 Sep 2025
  • Clinical dysmorphology
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic review.
  • 25 Sep 2025
  • Clinical dysmorphology
Recurrent herpes labialis in a patient with interferon regulatory factor 3 deletion: a novel case report.
  • 22 Sep 2025
  • Clinical dysmorphology
Observed total and live birth prevalence of Wolf-Hirschhorn syndrome in England 2015-2020.
  • 19 Sep 2025
  • Clinical dysmorphology

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