Clinical Dysmorphology

SCI期刊
Clinical Dysmorphology
中文名称:
临床形态学
期刊缩写:
CLIN DYSMORPHOL
影响因子:
0.4
ISSN:
print: 0962-8827
on-line: 1473-5717
研究领域:
医学-遗传学
创刊年份:
1992年
h-index:
27
自引率:
0.00%
Gold OA文章占比:
1.52%
原创研究文献占比:
84.09%
SCI收录类型:
Science Citation Index Expanded (SCIE) || Scopus (CiteScore)
期刊介绍英文:
Clinical Dysmorphology publishes succinct case reports on the etiology, clinical delineation, genetic mapping, and molecular embryology of birth defects. This journal covers such topics as multiple congenital anomaly syndromes - with particular emphasis on previously undescribed conditions, rare findings, ethnic differences in existing syndromes, fetal abnormalities, and cytogenetic aberrations that might give clues to the localization of developmental genes. Regular features include original, peer-reviewed articles, conference reports, book and software reviews, abstracts and summaries from the UK Dysmorphology Club, and literature summaries. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors wihtout further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
CiteScore:
CiteScoreSJRSNIPCiteScore排名
1.20.1860.363
学科
排名
百分位
大类:Medicine
小类:Pediatrics, Perinatology and Child Health
216 / 330
34%
大类:Medicine
小类:Anatomy
32 / 48
34%
大类:Medicine
小类:Pathology and Forensic Medicine
152 / 208
26%
大类:Medicine
小类:Genetics (clinical)
84 / 99
15%
发文信息
中科院SCI期刊分区
大类 小类 TOP期刊 综述期刊
4区 医学
4区 遗传学 GENETICS & HEREDITY
WOS期刊分区
学科分类
Q4GENETICS & HEREDITY
历年影响因子
2015年0.5180
2016年0.5730
2017年0.4270
2018年0.7600
2019年0.5210
2020年0.8160
2021年0.8840
2022年0.7000
2023年0.4000
历年发表
2012年61
2013年50
2014年42
2015年42
2016年43
2017年57
2018年46
2019年54
2020年71
2021年67
2022年64
投稿信息
出版周期:
Quarterly
出版语言:
English
出版国家(地区):
UNITED STATES
审稿时长:
6-12 weeks
出版商:
Lippincott Williams and Wilkins
编辑部地址:
LIPPINCOTT WILLIAMS & WILKINS, 530 WALNUT ST, PHILADELPHIA, USA, PA, 19106-3621

Clinical Dysmorphology - 最新文献

Nephrocalcinosis, distal renal tubular acidosis and skeletal abnormality in two siblings with ROGDI-related Kohlschütter-Tönz syndrome.

Pub Date : 2024-10-22 DOI: 10.1097/MCD.0000000000000509 Gayatri Nerakh, Swetha Koneru, Prashanth Rao Dhareneni

Thirteen Indians with camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Pub Date : 2024-10-01 DOI: 10.1097/MCD.0000000000000500 Swati Singh, Vaishnavi Ashok Badiger, Suma Balan, Sheela Nampoothiri, Anand Prahalad Rao, Hitesh Shah, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, Katta M Girisha

A case of U2AF2 -related developmental disorder: long-term follow-up and expansion of the phenotype.

Pub Date : 2024-10-01 DOI: 10.1097/MCD.0000000000000505 Muhammed Fatih Mulayim, Mustafa Hakan Demirbas, Ferda E Percin, Ebru Arhan, Gulsum Kayhan
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