PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers. - Wikidata - wikimedia - TriplyDB

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers.

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers.

http://www.wikidata.org/entity/Q37316953

about

Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.Advances in preimplantation genetic diagnosis/screening.BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD.Hereditary breast and ovarian cancer and reproduction: an observational study on the suitability of preimplantation genetic diagnosis for both asymptomatic carriers and breast cancer survivors.Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform.

P2860

Q27026343-03A0DD69-A2A4-4FF1-807E-2B95EE488196 Q34477384-6BDC29A4-4D43-42A7-9DD4-F80C68E3B553 Q34550417-21112D10-2382-4F57-8E7F-07EAB2F1B860 Q38218436-09786B88-9FA3-4725-B8E6-F15E0C25140D Q38613013-58644BA8-CB8D-404D-A569-10056D298DFB Q51145030-11D6FBCE-72C2-4D6E-9F0C-64191549D909 Q52655165-D1A7D73C-45CE-49F3-845C-9BCD45BED7AA

P2860

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers.

http://www.wikidata.org/entity/Q37316953

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 27 March 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@en

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@nl

type

label

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@en

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@nl

prefLabel

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@en

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@nl

P1433

Q37316953-61261A0F-3862-49F3-8658-9D5BD70A4F46

P1476

Q37316953-BA5EEAE7-5063-4705-81A3-EBA539727783

P2093

Q37316953-1731BB96-55EB-4D05-89D6-540E31A9A885

Q37316953-69CFBBEB-EDD7-412F-8F0C-319EE1DC327B

Q37316953-71E00C28-9F52-4A08-8DFF-1F23B7261AD2

Q37316953-932A0CCC-D620-4A26-9F76-9840AF9076C1

Q37316953-9E1C01B8-7F13-4AE3-A09D-73EE727B073E

Q37316953-A3AC13B9-F325-4140-9328-C3D6E6DF11B0

Q37316953-A6ED6E31-D18D-4B6F-A1FA-273409D07ED3

Q37316953-A83B77FE-A1EC-49DC-9A48-3047540A9DD0

Q37316953-B9306662-EFA7-4A6C-BA39-77863A1DA69C

Q37316953-BCDF7942-23A9-4ADE-9E7B-7A20364EFFA2

P2860

Q37316953-052B87F1-B415-4A3E-832C-2DBA9B4FCAE9

Q37316953-0B752C45-7EFF-4CC5-9C66-8AC17691B498

Q37316953-0BF99E93-A717-459C-A438-63EC5FA3DDF2

Q37316953-146F7168-481B-46FC-B92A-79CCB49F94CA

Q37316953-1FA7DCED-9297-4C73-95DA-CB0C19EAEDFE

Q37316953-44EC459A-B403-476A-B273-6FFFD67166C5

Q37316953-5A4632A4-F6EF-4A19-90AF-F0C0BB3CED3A

Q37316953-61FAC1CA-CCAC-479B-9BE8-5621884FA963

Q37316953-7649F385-EF2A-44C2-83F9-63571127E432

Q37316953-929ACE3C-DD35-4E69-8196-81EAF1D6F89C

P2888

Q37316953-20E9F1B0-A0E0-4203-91BF-12AD75195331

P304

Q37316953-13AAF915-FC15-4886-AEA8-615E3BFFAF8F

P31

Q37316953-ED5DFF2B-390A-4714-8216-F2D784561203

P356

Q37316953-4DC88C13-0710-4E4F-BDDF-DF66FF58790C

P433

Q37316953-4E8C6C50-D432-49EC-9503-F78A9E7CBC6A

P478

Q37316953-D3A49831-680D-445F-BD81-EC3AD71F7687

P577

Q37316953-63E5112B-DF82-4367-8F98-3D9493E65815

P5875

Q37316953-0AAF0A2D-E885-4136-984C-862C3B64DD8A

P698

Q37316953-A46547DB-A0C6-40A2-B16C-0AC17E1B61AF

P921

Q37316953-3A983A58-4226-4809-A2E0-0611F17B0908

P932

Q37316953-C5588605-689A-4BB3-B326-950FF5567988

P356

P1433

European Journal of Human Genetics

P1476

PGD for hereditary breast and ...... 1 and BRCA2 mutation carriers.

@en

P2093

Aimée D Paulussen

http://www.w3.org/2001/XMLSchema#string

Christine E de Die-Smulders

http://www.w3.org/2001/XMLSchema#string

Edith Coonen

http://www.w3.org/2001/XMLSchema#string

Encarna Gómez-García

http://www.w3.org/2001/XMLSchema#string

Hubert J Smeets

http://www.w3.org/2001/XMLSchema#string

Inge Derks-Smeets

http://www.w3.org/2001/XMLSchema#string

Jannie van Echten-Arends

http://www.w3.org/2001/XMLSchema#string

Joep P Geraedts

http://www.w3.org/2001/XMLSchema#string

Jos C Dreesen

http://www.w3.org/2001/XMLSchema#string

Marinus J Blok

http://www.w3.org/2001/XMLSchema#string

P2860

BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations

Proof of principle and first cases using preimplantation genetic haplotyping--a paradigm shift for embryo diagnosis

Identification of the breast cancer susceptibility gene BRCA2

Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families.

The relationship between the roles of BRCA genes in DNA repair and cancer predisposition.

Extending preimplantation genetic diagnosis: the ethical debate. Ethical issues in new uses of preimplantation genetic diagnosis.

A high proportion of founder BRCA1 mutations in Polish breast cancer families.

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.

Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population.

P2888

P304

1361-1368

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/EJHG.2013.50

http://www.w3.org/2001/XMLSchema#string

P433

12

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P577

2013-03-27T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

236083462

http://www.w3.org/2001/XMLSchema#string

P698

23531862

http://www.w3.org/2001/XMLSchema#string

P921

P932

3831069

http://www.w3.org/2001/XMLSchema#string