Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and PNPLA1[original query] |
---|
Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population. Cancer biomarkers : section A of Disease markers 2017 Oct . Lu Nanhang, Wang Jinzeng, Zhu Bijun, Zhang Miaomiao, Qi Fazhi, Wang Xiangdong, Gu Jianyi |
Novel and Recurrent PNPLA1 Mutations in Spanish Patients with Autosomal Recessive Congenital Ichthyosis; Evidence of a Founder Effect. Acta dermato-venereologica 2019 5 99 (10): 894-898. Esperón-Moldes Uxia, Ginarte Val Manuel, Rodríguez-Pazos Laura, Fachal Laura, Azaña José Manuel, Barberá Fons María, Viejo Diaz Mónica, Vega A |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: