Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1897-4287

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing ; volume:10 ; number:2 ; day:12 ; month:4 ; year:2012 ; pages:1 ; date:12.2012
Hereditary cancer in clinical practice ; 10, Heft 2 (12.4.2012), 1, 12.2012

Contributor: Blanc, R.
Jammot, A.
Nguyen-Dumont, T.
Teo, ZL
Odefrey, FA
Hammet, F.
Goldgar, DE
Park, DJ
Southey, MC
SpringerLink (Online service)

DOI: 10.1186/1897-4287-10-S2-A91

URN: urn:nbn:de:1111-2016073118021

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:44 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

Blanc, R.
Jammot, A.
Nguyen-Dumont, T.
Teo, ZL
Odefrey, FA
Hammet, F.
Goldgar, DE
Park, DJ
Southey, MC
SpringerLink (Online service)

Other Objects (12)

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

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.

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia

A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema

Related objects

Reset password