Advances in renal genetic diagnosis. - Wikidata - wikimedia - TriplyDB

Advances in renal genetic diagnosis.

Advances in renal genetic diagnosis.

http://www.wikidata.org/entity/Q38673027

about

Problems of unknown significance: Counseling in the era of next generation sequencing

P2860

Q58690880-3D06E122-EB0D-48D5-8AF9-39AB588D6193

P2860

Advances in renal genetic diagnosis.

http://www.wikidata.org/entity/Q38673027

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Advances in renal genetic diagnosis.

@en

type

label

Advances in renal genetic diagnosis.

@en

prefLabel

Advances in renal genetic diagnosis.

@en

P1433

Q38673027-E744E763-C39B-43E6-83AE-0E7704757BDC

P1476

Q38673027-DCA3CF6C-268A-4DF8-874B-C56B6E22BDC8

P2093

Q38673027-CE10D16F-8876-4BBD-AE88-3330A765A565

P2860

Q38673027-03CEB2F9-7CD5-4BB0-A5E9-2AC3FDCC3D5C

Q38673027-0728B4A8-4CBC-451F-A0FA-454EEE8C039D

Q38673027-0F76B4B7-AD0C-4B1F-A5EE-CE9751AF0B6B

Q38673027-127AFE56-DB98-41C8-82C5-109A57831DF1

Q38673027-33B0B375-0485-407E-B7A2-9DA6AC43B352

Q38673027-3493CAC1-1EFB-4E5A-AB2E-65A32EDF4827

Q38673027-3B7FFB50-D20E-4B26-A0EE-221CB0ECAE34

Q38673027-4EF0F375-7ACB-459F-BC6A-EF4309931B63

Q38673027-53AAAE69-B5FC-480C-9407-9B76098B18F7

Q38673027-5EC8C066-D4CB-49F3-B121-51EF8CCF35AC

P2888

Q38673027-B235C301-1F42-477D-8703-38F2C9F0788F

P304

Q38673027-1E38AD66-17D1-4B6C-A463-9470C957DCA5

P31

Q38673027-37C2A34E-E6A0-451B-9233-FD5B49B8B004

P356

Q38673027-73282480-4E6C-4250-A896-7EBE232E9B6F

P433

Q38673027-06CA9262-4A11-4227-9FDE-8DA007095726

P478

Q38673027-86E8FD70-A9DD-4D75-823C-15C9BAAEC764

P577

Q38673027-DF1A1E2C-D744-4F57-8D77-36748017E32B

P6179

Q38673027-73637B6A-1257-430B-B3FE-9E68F0849D30

P698

Q38673027-4055BC37-FC14-4851-A1DC-B81FDA060FDA

P356

S00441-017-2636-6

P1433

Cell and Tissue Research

P1476

Advances in renal genetic diagnosis.

@en

P2093

Carsten Bergmann

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

P2860

ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies

Sequencing technologies - the next generation

Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report

Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies.

Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.

Cardiovascular complications in atypical haemolytic uraemic syndrome.

Spectrum of complement-mediated thrombotic microangiopathies: pathogenetic insights identifying novel treatment approaches.

An international consensus approach to the management of atypical hemolytic uremic syndrome in children.

Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference.

Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease.

P2888

s00441-017-2636-6

P304

93-104

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

P31

scholarly article

P356

10.1007/S00441-017-2636-6

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

P433

1

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

P478

369

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

P577

2017-06-09T00:00:00Z

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

P6179

1085936661

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

P698

28597138

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