verified SJR 0,265 · Q3 • database Scopus / SJR & Web of Science indexed

United Kingdom · Lippincott Williams and Wilk...

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Clinical Dysmorphology

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.

ISSN: 0962-8827

Editorial: Lippincott Williams and Wilkins

Category: Medicine (miscellaneous)

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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schedule Datos CoP · solo campos en BD

SJR Impact Factor trending_up

0,265 Q3

H-index 33

Tasa de Aceptación pie_chart

36%

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

NPD Subscription

Ruta Non-OA NPD

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,265

H-index

Docs (year)

Docs 3y

133

Total refs

528

Cites 3y

Citable 3y

131

Cites/Doc 2y

0.52

Ref/Doc

12.57

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

A novel chromosomal aberration in a child with suspected Juberg-Hayward syndrome

Xq25 microduplication syndrome

Branchio-oculo-facial syndrome

Autosomal dominant inheritance of Williams???Beuren syndrome in a father and son with haploinsufficiency for FKBP6

Atypical, milder presentation in a child with CC2D2A and KIDINS220 variants

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

Anophthalmia in fronto-facial-nasal dysplasia

An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy

Absent digit in Russell-Silver syndrome

A rare cause of temple syndrome

A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type

A novel missense variant in the BBS7 gene underlying Bardet-Biedl syndrome in a consanguineous Pakistani family

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

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

A novel autosomal recessive DEAF1 nonsense variant

A new malformation syndrome with congenital arthrogryposis and severe hyperkeratosis

A neuropsychiatric disorder associated with dense calcification of the external ears and distal muscle wasting: ???Primrose syndrome???

A neuromuscular disorder with homozygosity for PIEZO2 gene variants

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

A distinct autosomal recessive disorder of limb development with preaxial brachydactyly, phalangeal duplication, symphalangism and hyperphalangism

A clinical report and further delineation of the 14q32 deletion syndrome

A case report of trisomy 17 mosaicism

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

3-methylglutaconic aciduria type IV

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