A familial dysmorphic condition with hypotonia, seizures and precocious puberty-Reference-Cited by-同舟云学术

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A familial dysmorphic condition with hypotonia, seizures and precocious puberty

Published:2008-07 Issue:3 Volume:17 Page:161-164
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Smith Audrey,Leask Kathryn,Tomlin Pamela,Donnai Dian

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetics and Epigenetics of Precocious Puberty;Russian Journal of Genetics;2023-12

2. Genetics and Epigenetics of Precocious Puberty;Генетика;2023-12-01

3. Klarigi: Characteristic explanations for semantic biomedical data;Computers in Biology and Medicine;2023-02

4. Identification of a novel pathogenic TBCK variant in a Chinese patient with infantile hypotonia with psychomotor retardation and characteristic facies type 3 (IHPRF3): a case report;BMC Pediatrics;2022-10-22

5. Further delineation of TBCK - Infantile hypotonia with psychomotor retardation and characteristic facies type 3;European Journal of Medical Genetics;2019-04

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