(Q28207518)

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Aplasia cutis congenita: a report of 12 new families and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Adams-Oliver syndrome: further evidence for autosomal recessive inheritance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Hereditary cranium bifidum and symmetric parietal foramina are the same entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Positional cloning of a gene involved in hereditary multiple exostoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Adams-Oliver syndrome revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Adams Oliver syndrome: a family with extreme variability in clinical expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Limb defects with cutis marmorata teleangiectatica congenita: Adams-Oliver syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Adams-Oliver syndrome: aplasia cutis congenita, terminal transverse limb defects and cutis marmorata telangiectatica congenita.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Cerebral cortical dysplasia and digital constriction rings in Adams-Oliver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome-McKusick 10030): further suggestion of autosomal recessive inheritance

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Further family with possible autosomal recessive inheritance of Adams-Oliver syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Adams-Oliver syndrome associated with cardiovascular malformations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Vascular pathogenesis of transverse limb reduction defects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams-Oliver syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Adams-Oliver syndrome: cutis marmorata teleangiectatica congenita with multiple anomalies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Vascular abnormalities in Adams-Oliver syndrome: Cause or effect?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200980

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200980

1 reference

Consolidated OpenCitations Corpus – April 2017

release_zq672jn2ujcyheymnabuodbfx4

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zq672jn2ujcyheymnabuodbfx4

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12774039

1 reference

Consolidated OpenCitations Corpus – April 2017