Chromosome 11q13 deletion syndrome. - Wikidata - awgldk - TriplyDB

Chromosome 11q13 deletion syndrome.

Chromosome 11q13 deletion syndrome.

http://www.wikidata.org/entity/Q39676379

about

Chromosome 11q13 deletion syndrome.

http://www.wikidata.org/entity/Q39676379

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Chromosome 11q13 deletion syndrome.

@en

Chromosome 11q13 deletion syndrome.

@nl

type

label

Chromosome 11q13 deletion syndrome.

@en

Chromosome 11q13 deletion syndrome.

@nl

prefLabel

Chromosome 11q13 deletion syndrome.

@en

Chromosome 11q13 deletion syndrome.

@nl

P1433

Q39676379-CBC38C16-1D14-43B3-8011-0757A9E8DBE9

P1476

Q39676379-94A070A9-0F34-4B27-B6D7-D1BF6FB91DD7

P2093

Q39676379-51F78A4A-4CA8-4939-BA90-1B57C11A2D20

Q39676379-A81ED774-8147-4AEA-ABF8-E6067670A6C4

Q39676379-E118CFB1-20B7-491B-AD55-A6134D61B0FC

Q39676379-F56D3E77-A37B-4704-86FE-00D6E9366CCA

P2860

Q39676379-0566B5BA-67BD-4988-9EE4-6B525B615CA7

Q39676379-07E10396-A93D-4BB9-BCC9-1A21F606CA77

Q39676379-12FE4893-29E7-4519-AF64-6A310EA98282

Q39676379-195A04FF-6B7C-440E-8E6E-B1ECBA68336D

Q39676379-397BFE6A-B0E4-4E26-AC2E-B78885632231

Q39676379-51D2097B-BCE3-4E8C-80C7-4672699C2EBD

Q39676379-60A4C8C2-161F-444F-9A29-D72E46E32A01

Q39676379-682A02D5-237F-44D9-BEB7-0510C00A0561

Q39676379-9F33A447-DFEF-4064-B23E-3E66FAAB5ED4

Q39676379-A1374A4A-1DA6-4829-B2AA-982D3641D554

P304

Q39676379-AA25D741-446A-4004-95B8-911A6A4D7884

P31

Q39676379-86E26AA1-23AD-45A2-8C2C-904AEA68A67F

Q39676379-8eb0f385-b4e8-4fea-a011-26c65cfbe066

P356

Q39676379-E3ED0BEC-0443-44AB-BB1A-BCC952A6B4FC

P433

Q39676379-C7B9DD99-37F2-4469-8CDC-404BCB963674

P478

Q39676379-24C64282-09B4-4BFF-A96D-AB9EA9EE9707

P50

Q39676379-58502E8F-AB6E-4E48-AA64-385EAD2541CD

P577

Q39676379-DE80A189-235F-403A-9060-B4D20E45B9E7

P698

Q39676379-E1423C98-CDE9-47A0-93C7-1FA5CC152CD9

P932

Q39676379-5462D5D1-91D0-49A9-AF1A-715A91ADE096

P356

KJP.2016.59.11.S10

P1433

Korean journal of pediatrics

P1476

Chromosome 11q13 deletion syndrome

@en

P2093

Baik-Lin Eun

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

Gun-Ha Kim

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

So-Hee Eun

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

Yu-Seon Kim

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

P2860

Otodental syndrome

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma

Otodental syndrome: a case report and genetic considerations.

The association of ocular defects with the otodental syndrome.

Otodental syndrome. A case report.

"Otodental" dysplasia.

Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype

A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.

Otodental dysplasia: a "new" ectodermal dysplasia.

P304

S10-S13

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

P31

scholarly article

P356

10.3345/KJP.2016.59.11.S10

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

P433

Suppl 1

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

P478

59

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

P50

P577

2016-11-30T00:00:00Z

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

P698

28018436

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

P932

5177688

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