Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

about

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

Item

http://www.wikidata.org/entity/Q53262754

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@en

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@nl

type

Item

label

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@en

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@nl

prefLabel

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@en

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@nl

P1476

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.

@en

P2093

Dino Colo

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

Isabel N Tromp

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

Jelle F Homans

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

Moyo C Kruyt

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

René M Castelein

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

Terrence B Crowley

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

Tom P C Schlösser

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

Vincent F X Deeney

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

P2860

Cardiofacial syndrome. Congenital heart disease and facial weakness, a hitherto unrecognized association

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement

Practical guidelines for managing patients with 22q11.2 deletion syndrome

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH

Tools for assessing quality and susceptibility to bias in observational studies in epidemiology: a systematic review and annotated bibliography

Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.

P31

scholarly article

P356

10.1002/AJMG.A.38545

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

P407

English

P50

Donna M McDonald-McGinn

P577

2017-11-21T00:00:00Z

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

P698

29159873

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