Literature DB >> 5538320

Recognizable patterns of human malformation: genetic, embryologic, and clinical aspects.

D W Smith.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 5538320

Source DB:  PubMed          Journal:  Major Probl Clin Pediatr        ISSN： 0076-2865


× No keyword cloud information.
  4 in total

1.  FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.

Authors:  Juan Wang; Jinling Liu; Qingjiong Zhang
Journal:  Mol Vis       Date:  2007-01-26       Impact factor: 2.367

2.  Oculomandibular dyscephaly (Hallermann-Streiff-François syndrome) associated with epilepsy.

Authors:  L Crevits; E Thiery; H van der Eecken
Journal:  J Neurol       Date:  1977-06-13       Impact factor: 4.849

Review 3.  Phalangeal Intra-Articular Osteochondroma Caused a Rare Clinodactyly Deformity in Children: Case Series and Literature Review.

Authors:  Yun Hao; Jia-Chao Guo; Xiao-Lin Wang; Jing-Fan Shao; Jie-Xiong Feng; Jin-Peng He
Journal:  Front Endocrinol (Lausanne)       Date:  2021-08-12       Impact factor: 5.555

4.  Correlational research on facial and clinical characteristics of adolescents with obsessive-compulsive disorder.

Authors:  Yan-Rong Wang; Shao-Hua Chang; Xiao-Min Ma; Ji-Ying Li; Rui-Xia Zhang; Jian-Qun Fang
Journal:  BMC Psychiatry       Date:  2021-12-11       Impact factor: 3.630
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.