Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing ; volume:11 ; number:1 ; day:13 ; month:1 ; year:2021 ; pages:1-7 ; date:12.2021
Scientific reports ; 11, Heft 1 (13.1.2021), 1-7, 12.2021

Creator: Kim, Boram
Kim, Man Jin
Hur, Keunyoung
Jo, Seong Jin
Ko, Jung Min
Park, Sung Sup
Seong, Moon-Woo
Mun, Je-Ho

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-020-80867-0

URN: urn:nbn:de:101:1-2021020800203495788922

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:22 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Kim, Boram
Kim, Man Jin
Hur, Keunyoung
Jo, Seong Jin
Ko, Jung Min
Park, Sung Sup
Seong, Moon-Woo
Mun, Je-Ho
SpringerLink (Online service)

Other Objects (12)

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Whole-exome sequencing of a pedigree segregating asthma

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Comprehensive comparison of three commercial human whole-exome capture platforms

Human whole-exome genotype data for Alzheimer’s disease

Genomic alterations in gastric cancers discovered via whole-exome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Related objects

Reset password