Cover Image

Investigation of Genetic Mutations in High-risk and Low-risk Basal Cell Carcinoma in a Non-Caucasian Population by Whole Exome Sequencing

This study analysed genomic mutations in basal cell carcinoma using whole exome sequencing of DNA specimens obtained from 20 Korean patients. Histological evaluation determined that 15 (75%) were low-risk basal cell carcinomas, and 5 (25%) were high-risk basal cell carcinomas. Seventy-five percent o...

Full description

Saved in:

Bibliographic Details
Main Authors:	Hyun Jee Kim (Author), Minho Lee (Author), Young Bok Lee (Author), Dong Soo Yu (Author)
Format:	Book
Published:	Medical Journals Sweden, 2021-05-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Whole-exome sequencing reveals ANO8 as a genetic risk factor for intrahepatic cholestasis of pregnancy
by: Xianxian Liu, et al.
Published: (2020)

Whole exome sequencing identifies a novel FRAS1 mutation and aids in vitro fertilization with preimplantation genetic diagnosis in Fraser syndrome
by: Tsung-Ying Ou, et al.
Published: (2022)

Mapping of the mutational landscape of Juvenile Myelomonocytic Leukemia patients by whole exome sequencing
by: Aditya Kumar Gupta, et al.
Published: (2024)

mutations in identified by whole exome sequencing in 2 girls with Alport syndrome in Korea
by: Kyoung Hee Han, et al.
Published: (2019)

Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay
by: Ji Yoon Han, et al.
Published: (2020)

Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome.
by: Victor Borda, et al.
Published: (2021)

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration
by: Dae Joong Ma, et al.
Published: (2021)

An atypical case of Noonan syndrome with mutation diagnosed by targeted exome sequencing
by: Jinsup Kim, et al.
Published: (2017)

Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing
by: Bo-Young Kim, et al.
Published: (2017)

Case report: mutation analysis of primary pulmonary lymphoepithelioma-like carcinoma via whole-exome sequencing
by: Hong Xuan, et al.
Published: (2019)

Clinical use of whole exome sequencing in children with developmental delay/intellectual disability
by: Yoon Hee Jo, et al.
Published: (2024)

Refractory Seizure with Autosomal Dominant Hypocalcemia with Hypercalciuria with a Mutation Detected Using Whole Exome Sequencing
by: Seong Bae Ahn, et al.
Published: (2021)

Genetic analysis using whole-exome sequencing in pediatric chronic kidney disease: a single center's experience
by: Hyeonju Lee, et al.
Published: (2022)

Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management
by: Jiwon Jung, et al.
Published: (2021)

Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
by: Yingjie Zhou, et al.
Published: (2020)

Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases
by: Vianey Ordoñez-Labastida, et al.
Published: (2022)

Exome-wide survey of the Siberian Caucasian population
by: Andrey A. Yurchenko, et al.
Published: (2019)

The first Korean case with Floating-Harbor syndrome with a novel mutation diagnosed by targeted exome sequencing
by: Eun Mi Choi, et al.
Published: (2018)

The identification of novel gene mutations for degenerative lumbar spinal stenosis using whole-exome sequencing in a Chinese cohort
by: Xin Jiang, et al.
Published: (2021)

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report
by: Hye Ji Choi, et al.
Published: (2017)

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
by: Gordon K C Leung, et al.
Published: (2018)

Whole Exome Sequencing of Chronic Myeloid Leukemia Patients
by: Shaghayegh SABRI, et al.
Published: (2016)

Whole-exome sequencing of a pedigree segregating asthma
by: DeWan Andrew T, et al.
Published: (2012)

Identification of potential causal variants for premature ovarian failure by whole exome sequencing
by: Haengun Jin, et al.
Published: (2020)

Genomic landscape of hepatocellular carcinoma in Egyptian patients by whole exome sequencing
by: Perihan Hamdy Kassem, et al.
Published: (2024)

Whole‐exome sequencing analysis of juvenile papillomatosis and coexisting breast carcinoma
by: Timothy M D'Alfonso, et al.
Published: (2021)

Whole exome sequencing of benign pulmonary metastasizing leiomyoma reveals mutation in the BMP8B gene
by: Deniss Sõritsa, et al.
Published: (2018)

Genetic analysis of 280 children with unexplained developmental delay or intellectual disability using whole exome sequencing
by: Jinbo Xu, et al.
Published: (2024)

A Case of Mitochondrial Trifunctional Protein Deficiency with Variants Diagnosed Using Whole-Exome Sequencing
by: Chan Kim, et al.
Published: (2021)

Whole exome sequencing analysis of 167 men with primary infertility
by: Haiyan Zhou, et al.
Published: (2024)

Correction: Genomic landscape of hepatocellular carcinoma in Egyptian patients by whole exome sequencing
by: Perihan Hamdy Kassem, et al.
Published: (2024)

Whole-exome sequencing reveals the etiology of the rare primary hepatic mucoepidermoid carcinoma
by: Ping Hou, et al.
Published: (2021)

Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature
by: Zilong Qiu, et al.
Published: (2022)

Identification of potential pathogenic mutations in Chinese children with first branchial cleft anomalies detected by whole‐exome sequencing
by: Yeran Yang, et al.
Published: (2021)

Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome
by: Chao Ling, et al.
Published: (2019)

Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature
by: Ben Pode-Shakked, et al.
Published: (2019)

Case Report: Identification of Polygenic Mutations by Exome Sequencing
by: Yanfeng Liu, et al.
Published: (2021)

Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability
by: Chunyan Jin, et al.
Published: (2021)

Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing
by: Hu X, et al.
Published: (2021)

Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome
by: Talal J. Qazi, et al.
Published: (2020)