ISSN: 0962-8827
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Clinical Dysmorphology Q3 Unclaimed
Clinical Dysmorphology is a journal indexed in SJR in Medicine (miscellaneous) and Pathology and Forensic Medicine with an H index of 33. It has an SJR impact factor of 0,186 and it has a best quartile of Q3. It has an SJR impact factor of 0,186.
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Publication frecuency: -


- €
Inmediate OANPD
Embargoed OA- €
Non OAMetrics
0,186
SJR Impact factor33
H Index41
Total Docs (Last Year)142
Total Docs (3 years)565
Total Refs73
Total Cites (3 years)140
Citable Docs (3 years)0.38
Cites/Doc (2 years)13.78
Ref/DocOther journals with similar parameters
Swiss Medical Weekly Q3
Neurologia Q3
Canadian Journal of Experimental Psychology Q3
Journal of Physiology and Pharmacology Q3
Revista do Instituto de Medicina Tropical de Sao Paulo Q3
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Aims and Scope
Best articles by citations
Xq25 microduplication syndrome
View moreA girl with a neurodevelopmental syndrome, adducted thumbs and frequent infections caused by novel homozygous variant in DEAF1
View moreHip dislocation in 3-M syndrome
View moreA rare cause of temple syndrome
View moreChondrodysplasia punctata tibia metacarpal type
View moreCutis laxa and fatal pulmonary hypertension
View moreDK-phocomelia syndrome with thrombocytopenia, encephalocele, and choanal atresia in an adult male with moderate learning difficulties
View moreTFAP2A mutation in a child and mother with predominantly ocular anomalies
View moreA case report of trisomy 17 mosaicism
View moreMild presentation of the congenital variant Rett syndrome in a Pakistani male
View moreA novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis
View moreBranchio-oculo-facial syndrome
View more16p13.11-p12.3 Microdeletion identified in a patient with sagittal craniosynostosis and developmental delay
View moreBranchiootorenal syndrome with skeletal defects
View moreAtypical osteogenesis imperfecta caused by a 17q21.33 deletion involving COL1A1
View moreEarly diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement
View moreReport of a family with craniofrontonasal syndrome
View moreScalp lesions in Turner syndrome: a result of lymphoedema?
View moreThree new cases with a supernumerary ring chromosome 1
View moreA boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1
View moreCardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation
View moreScalp skin lesion in Turner syndrome: more than lymphoedema?
View moreHajdu-Cheney syndrome
View moreRaine dysplasia: a Brazilian case with a mild radiological involvement
View more
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