Clinical Dysmorphology

Published by Wolters Kluwer - Lippincott Williams & Wilkins

United Kingdom · Genomic variations and chromosomal abnormalities

Journal at a glance

ISSN

14735717

Publisher

Wolters Kluwer - Lippincott Williams & Wilkins

Country

United Kingdom

Language

en

Also known as: Clin Dysmorphol (Abbreviation)

Indexing

• Web of Science (SCIE): Indexed
• Scopus: Indexed
• Medline: Active
• Pubmed: Active

Metrics

Subjects

• Genomic variations and chromosomal abnormalities
• Craniofacial Disorders and Treatments
• Connective tissue disorders research
• Congenital limb and hand anomalies
• Prenatal Screening and Diagnostics
• Genomics and Rare Diseases
• Hedgehog Signaling Pathway Studies

Articles on PubPorta

The most recent records PubPorta holds for this journal.

• Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases (2026)
• 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 (2026)
• Lateral nasal proboscis associated with nasal glioma: a complex unilateral craniofacial malformation (2026)
• A rare RASopathy: Noonan syndrome-like disorder with loose anagen hair caused by a protein phosphatase 1 catalytic subunit beta pathogenic variant (2026)
• Homozygous intragenic deletion of breast carcinoma–amplified sequence 3 in Hengel–Maroofian–Schols syndrome: expanding the clinical and molecular spectrum (2026)

Similar journals

• Journal of Medical Genetics — United Kingdom · — · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total, Same country
• Genetics in Medicine Open — Open access · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• European Journal of Medical Genetics — France · — · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• Molecular Genetics and Genomic Medicine — United States · Open access · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• Clinical Genetics — United Kingdom · — · Same subject: Genomic variations and chromosomal abnormalities, Same subject: Genomics and Rare Diseases, 3 shared subjects in total, Same country
• Clinical Genetics — United Kingdom · — · Same subject: Genomic variations and chromosomal abnormalities, Same subject: Genomics and Rare Diseases, 3 shared subjects in total, Same country

Sources: OpenAlex, NLM Catalog, Crossref, Web of Science (Clarivate), Scopus · Last verified 2026-09-05

Journal homepage