CLINICAL DYSMORPHOLOGY

简称 CLIN DYSMORPHOL ·UNITED STATES ·出版周期 Quarterly ·年均收录 40 篇

0.5

最新影响因子

4.20%

自引率

容易

投稿难度

较慢,6-12周

审稿周期

期刊简介

CLINICAL DYSMORPHOLOGY是一本专注于临床畸形学研究的国际期刊，ISSN号为0962-8827，由英国出版商Lippincott Williams & Wilkins出版，出版地为英国，出版周期为季刊。该期刊的影响因子较低，具体数值需查阅最新JCR报告，目前未被列为开放获取（OA）期刊，但被SCI收录，中科院分区情况需根据最新分区表确认。杂志的发文特点集中于先天性畸形、遗传综合征、形态异常等临床与遗传学相关研究，尤其关注病例报告和临床观察。其研究领域涵盖儿科、遗传学、畸形学及临床诊断。杂志质量较为专业，但因影响因子不高，学术影响力有限，适合特定领域的研究者投稿，需注意其受众较窄可能导致的引用率较低风险。

影响因子趋势

近期发表

Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant 2026-09-15

A novel homozygous frameshift variant in DYM causing Dyggve–Melchior–Clausen syndrome: expansion of the mutational spectrum 2026-09-15

Omphalocele–exstrophy–imperforate anus–spinal defects complex associated with a very rare limb anomaly mimicking polymelia 2026-09-15

Monochorionic dizygotic twins with discordant genetic findings and congenital malformations 2026-08-07

Generalized overgrowth in CDC42BPB-related Chilton-Okur-Chung neurodevelopmental syndrome: expanding the phenotypic spectrum 2026-08-07

Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion 2026-08-07

Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features 2026-03-12

Endocrine-predominant type 2 Woodhouse–Sakati syndrome caused by a novel homozygous DCAF17 variant 2026-03-12

A male infant with a novel heterogeneous nuclear ribonucleoprotein H1 variant, bilateral cataracts, dysplastic thumbs, and severe airway malacia 2026-03-12

Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four cases 2026-05-08