(Q28252346)

1

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Deborah Ruddy

2

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Wim Wuyts

4

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Margo Whiteford

5

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Diana Johnson

6

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Wayne Lam

7

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Richard C Trembath

American Journal of Medical Genetics Part A

8

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language of work or name

English

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publication date

August 2009

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published in

1 reference

Transverse limb defects associated with aorto-pulmonary vascular abnormalities: vascular disruption sequence or atypical presentation of Adams-Oliver syndrome?

PubMed

volume

149A

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issue

8

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page(s)

1860-81

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Congenital scalp defects: Adams-Oliver syndrome. A case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Aplasia cutis cerebri with partial acrania--total reconstruction in a severe case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Autosomal recessive type of Adams-Oliver syndrome: prenatal diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Autosomal dominant inheritance of scalp defects with ectrodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Acrania: a manifestation of the Adams-Oliver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Near fatal haemorrhage from the superior sagittal sinus in Adams-Oliver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

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/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome: a case with juvenile chronic myelogenous leukemia and chylothorax

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome associated with cutis marmorata telangiectatica congenita and congenital cataract: a case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Aplasia cutis congenita: a clinical review and proposal for classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Congenital scalp defect with distal limb reduction anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Hypoxia induces cardiac malformations via A1 adenosine receptor activation in chicken embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome and hepatoportal sclerosis: Occasional association or common mechanism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Teratogen-induced limb defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Congenital heart defect in a Japanese girl with Adams-Oliver syndrome: one of the most important complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of three additional cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Association of Adams-Oliver syndrome with pulmonary arterio-venous malformation in the same family: a further support to the vascular hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Limb deficiencies in newborn infants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams-Oliver syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

A case of Adams-Oliver syndrome with associated brain and pulmonary involvement: further evidence of vascular pathology?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome: genetics and associated anomalies of cutis aplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Aplasia cutis congenita, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Aplasia cutis congenita, congenital heart lesions, and frontonasal cysts in four successive generations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome with unusual central nervous system alterations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Recognition of thalidomide defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome: further evidence of an autosomal recessive variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Clinical and molecular analysis of nine families with Adams-Oliver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

The effect of hypoxia in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

Adams-Oliver syndrome revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32708

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.32708

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

980971

OpenCitations bibliographic resource ID

980971

1 reference