Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes. - Wikidata - wikimedia - TriplyDB

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

http://www.wikidata.org/entity/Q37010905

about

Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome.

P2860

Q30356916-8307525C-8BFA-48DD-ACD0-B7BD66C12A52

P2860

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

http://www.wikidata.org/entity/Q37010905

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 16 June 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Two maternal duplications invo ...... contrasting growth phenotypes.

@en

Two maternal duplications invo ...... contrasting growth phenotypes.

@nl

type

label

Two maternal duplications invo ...... contrasting growth phenotypes.

@en

Two maternal duplications invo ...... contrasting growth phenotypes.

@nl

prefLabel

Two maternal duplications invo ...... contrasting growth phenotypes.

@en

Two maternal duplications invo ...... contrasting growth phenotypes.

@nl

P1433

Q37010905-11A7139D-B549-48F9-8E81-A2282D6210F6

P1476

Q37010905-B3B37CCE-D829-4DF6-B052-CEB60EBABF7C

P2093

Q37010905-1B1C6C2C-06E9-42E3-B9DA-9E11C7109462

Q37010905-372F0DC6-5BE0-4E2D-8F63-4E800E0C6C4D

Q37010905-3B52C5A7-EA2F-43C7-98A6-77B0E233CDA7

Q37010905-6A556830-B099-42BE-B05F-3AB72846F1B6

Q37010905-93361F1A-D8CC-472D-BCAD-92BE479E37C8

Q37010905-BEEDBE18-DC24-4E88-9848-2C4FCA98873C

Q37010905-D5F17ED2-E1AD-493F-94C0-28DDED4D25EB

P2860

Q37010905-0B4BCCC9-3936-4870-9985-9A1CCACCFB0E

Q37010905-0E27EB7B-BDCD-4501-950D-95C66D78CF43

Q37010905-0F8CC275-2C47-4804-8451-A9A2C81E5692

Q37010905-14ACD898-99A7-4EA1-B449-70F985915C4A

Q37010905-1C1310AB-6463-4BF9-89A8-C9DC9672257E

Q37010905-25F261ED-CAA7-4E74-BF83-134A9802495F

Q37010905-298852F6-1C08-45AB-BAF4-E3D4C4F944AB

Q37010905-2B0C678D-7ABF-4C99-B025-EEAB06DBECC0

Q37010905-4A45A153-872D-4D4F-B303-3B50B8FFABD6

Q37010905-5236C67F-0E56-4FAA-8452-294EA5B7F04B

P2888

Q37010905-E2B9E77A-980C-41DA-93EA-0DC45472A278

P304

Q37010905-20EDF9D6-2EA2-461E-AD69-744DB22980A0

P31

Q37010905-2A617C2A-724C-4C7A-8C09-C1946E3F9114

Q37010905-86cd250a-dd5e-4b82-8e04-c8e582819302

P356

Q37010905-B8F7A108-C1C4-4B45-91C6-FBA5A7C5233C

P478

Q37010905-A5A2BA3E-25D3-4F6C-B8AC-5AD08B8DE8E3

P50

Q37010905-066C9A4F-FF51-4AE8-98D0-E097E0985564

Q37010905-3456630E-F4D5-469A-9131-12322FDD03D8

Q37010905-9B6EAB72-06E0-49EC-AB1D-999F1F4C81AF

Q37010905-B93301B0-BCBD-4FEE-88EE-F67471D9D5A1

Q37010905-F8F94FE1-71F1-44AA-A0A5-C333CABAF367

P577

Q37010905-04C2D7F9-FF3A-400B-9378-FACADC55513D

P6179

Q37010905-883D2BFD-FD17-43F5-B144-FB4D95218C6F

P698

Q37010905-A4350F7E-A03C-4AFB-8CC7-39DAB2CF9021

P932

Q37010905-BD706A18-5B7C-46E7-9C8A-77EC036BC550

P356

S13148-016-0236-Z

P1433

Clinical epigenetics

P1476

Two maternal duplications invo ...... contrasting growth phenotypes

@en

P2093

Andrea Freschi

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

Angela Sparago

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

Dorte Launholt Lildballe

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

Federica Maria Valente

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

Lucia Perone

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

Rikke Christensen

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

Susanne Eriksen Boonen

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

P2860

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases

Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight

Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature.

The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome.

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.

P2888

s13148-016-0236-z

P304

69

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

P31

scholarly article

P356

10.1186/S13148-016-0236-Z

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

P478

8

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

P50

Massimo Carella

P577

2016-06-16T00:00:00Z

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

P6179

1051100062

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

P698

27313795

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

P932

4910218

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