Author:
Naik Prashant,Kini Pushpa,Chopra Deepti,Gupta Yogesh
Subject
Genetics(clinical),Genetics
Reference37 articles.
1. The Finlay-Marks (SEN) syndrome: Report of a new case and review of the literature;Aase;Proc Greenwood Genet Center,1988
2. [Amastia and athelia as an exceptional presentation of hypohydrotic ectodermal dysplasia in an adolescent female.] [Article in Spanish];Alcón Saez;An Pediatr (Barc),2008
3. Hypotonia, developmental delay and features of scalp-ear-nipple syndrome in an inbred Arab family;Al-Gazali;Clin Dysmorphol,2007
4. [Hypohydrotic ectodermal dysplasia, a clinical case and review of the literature] [Article in Spanish];Aranibar;Rev Chil Pediatr,2005
5. PTPRF is disrupted in a patient with syndromic amastia;Ausavarat;BMC Med Genet,2011
Cited by
11 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. Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies;International Journal of Molecular Sciences;2024-05-09
2. Oral Mucosa and Nails in Genodermatoses: A Diagnostic Challenge;Journal of Clinical Medicine;2021-11-19
3. Disorders of Hair;Atlas of Dermatology, Dermatopathology and Venereology;2021-10-31
4. The phenotypic characteristics of patients with athelia and tooth agenesis;Annals of Translational Medicine;2021-10
5. Disorders of Hair;Atlas of Dermatology, Dermatopathology and Venereology;2021