Journal of pediatric genetics

Journal of pediatric genetics
影响因子:
0.4
ISSN:
print: 2146-4596
on-line: 2146-460X
研究领域:
PEDIATRICS
自引率:
0.00%
Gold OA文章占比:
0.60%
原创研究文献占比:
58.33%
SCI收录类型:
Emerging Sources Citation Index (ESCI)
期刊介绍英文:
The Journal of Pediatric Genetics is an English multidisciplinary peer-reviewed international journal publishing articles on all aspects of genetics in childhood and of the genetics of experimental models. These topics include clinical genetics, molecular genetics, biochemical genetics, medical genetics, dysmorphology, teratology, genetic counselling, genetic engineering, formal genetics, neuropsychiatric genetics, behavioral genetics, community genetics, cytogenetics, hereditary or syndromic cancer genetics, genetic mapping, reproductive genetics, fetal pathology and prenatal diagnosis, multiple congenital anomaly syndromes, and molecular embryology of birth defects. Journal of Pediatric Genetics provides an in-depth update on new subjects and current comprehensive coverage of the latest techniques used in the diagnosis of childhood genetics. Journal of Pediatric Genetics encourages submissions from all authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, short report, rapid communications, case reports, letters to the editor, and book reviews. The aim of the journal is to share and disseminate knowledge between all disciplines in the field of pediatric genetics. This journal is a publication of the World Pediatric Society: http://www.worldpediatricsociety.org/ The Journal of Pediatric Genetics is available in print and online. Articles published ahead of print are available via the eFirst service on the Thieme E-Journals platform.
发文信息
WOS期刊分区
学科分类
Q4PEDIATRICS
历年影响因子
2022年0.4000
2023年0.4000
历年发表
2012年12
2013年16
2014年1
2015年123
2016年40
2017年54
2018年42
2019年70
2020年128
2021年77
2022年32
投稿信息
出版国家(地区):
Germany
出版商:
Georg Thieme Verlag

Journal of pediatric genetics - 最新文献

Erratum: Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.

Pub Date : 2024-07-09 DOI: 10.1055/s-0044-1788343 Francisco Cammarata-Scalisi, Uta Matysiak, Colin E Willoughby, Gunda Ruzaike, Antonio Cárdenas Tadich, Maykol Araya Castillo, Carmen Zara-Chirinos, Ana Bracho, Andrea Avendaño, Houweyda Jilani, Michele Callea

Contributing Reviewers in 2023.

Pub Date : 2024-04-01 DOI: 10.1055/s-0044-1782623

A Novel Autosomal Recessive Candidate Gene Responsible for RASopathy-Like Phenotype and Bone Marrow Failure: RASA3

Pub Date : 2023-10-26 DOI: 10.1055/s-0043-1771526 Akif Ayaz, Zeynep Doğru, Kıvanç Kök, Nihan Bayram, Yöntem Yaman, Abdullah Hüseyin Köseoğlu, Türkan Yiğitbaşı, Aslı Güner Öztürk Demir, Elçin Yüksel, Burcu Dundar, Erdal Fırat Çaralan, Serdar Nepesov, Murat Elli
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