ISSN: 0962-8827

Journal Home

Journal Guideline

Clinical Dysmorphology Q3 Unclaimed

Lippincott Williams and Wilkins United Kingdom

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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 0,265 and it has a best quartile of Q3. It has an SJR impact factor of 0,265.

Type: Journal

Type of Copyright:

Languages:

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Anatomy (Q3) Medicine (miscellaneous) (Q3) Pathology and Forensic Medicine (Q3) Pediatrics, Perinatology and Child Health (Q3) Genetics (clinical) (Q4)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,265

SJR Impact factor

33

H Index

42

Total Docs (Last Year)

133

Total Docs (3 years)

528

Total Refs

80

Total Cites (3 years)

131

Citable Docs (3 years)

0.52

Cites/Doc (2 years)

12.57

Ref/Doc

Comments

No comments ... Be the first to comment!

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID *

* The email or ORCID field is only to validate the authenticity of the comment, the identity will not be public. .

Other journals with similar parameters

Canadian Respiratory Journal Q3
Current Stem Cell Research and Therapy Q3
Polish Journal of Microbiology Q3
JMIR Research Protocols Q3
Deutsches AÃàrzteblatt international Q3

Compare this journals

Aims and Scope

Best articles by citations

Xq25 microduplication syndrome

A girl with a neurodevelopmental syndrome, adducted thumbs and frequent infections caused by novel homozygous variant in DEAF1

Hip dislocation in 3-M syndrome

A rare cause of temple syndrome

Chondrodysplasia punctata tibia metacarpal type

Cutis laxa and fatal pulmonary hypertension

DK-phocomelia syndrome with thrombocytopenia, encephalocele, and choanal atresia in an adult male with moderate learning difficulties

TFAP2A mutation in a child and mother with predominantly ocular anomalies

A case report of trisomy 17 mosaicism

Mild presentation of the congenital variant Rett syndrome in a Pakistani male

A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis

Branchio-oculo-facial syndrome

SHOW MORE ARTICLES

16p13.11-p12.3 Microdeletion identified in a patient with sagittal craniosynostosis and developmental delay

Branchiootorenal syndrome with skeletal defects

Atypical osteogenesis imperfecta caused by a 17q21.33 deletion involving COL1A1

Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement

Report of a family with craniofrontonasal syndrome

Scalp lesions in Turner syndrome: a result of lymphoedema?

Three new cases with a supernumerary ring chromosome 1

A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1

Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation

Scalp skin lesion in Turner syndrome: more than lymphoedema?

Hajdu-Cheney syndrome

Raine dysplasia: a Brazilian case with a mild radiological involvement