The Peters' plus syndrome: a review (Q34525318)

2 August 2017

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title

The Peters' plus syndrome: a review (English)

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2 August 2017

author name string

Liesbeth J J M Maillette de Buy Wenniger-Prick

series ordinal

1

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2 August 2017

Raoul C M Hennekam

series ordinal

2

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2 August 2017

publication date

1 April 2002

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2 August 2017

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2 August 2017

volume

45

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2 August 2017

issue

2

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2 August 2017

page(s)

97-103

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Peters'-plus: a new syndrome

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Peters' anomaly as a consequence of genetic and nongenetic syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

The occurrence of congenital keratoconus posticus circumscriptus in two siblings presenting a previously unrecognized syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation—A new syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Japanese girl with Krause-van Schooneveld-Kivlin syndrome: Peters anomaly with short-limb dwarfism: Peter-Plus syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Posterior keratoconus associated with systemic abnormalities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

A child with sclerocornea, short limbs, short stature, and distinct facial appearance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Dwarfism, rhizomelic limb shortness, and abnormal face: new short stature syndrome sharing some manifestations with Robinow syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Robinow syndrome with developmental brain dysplasia.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Heterogeneity in dominant anterior segment malformations

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Autosomal dominant cataracts and Peters anomaly in a large Australian family.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Variable expressivity of autosomal dominant microcornea with cataract

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Dominant syndrome with isolated cryptophthalmos and ocular anomalies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Peters' anomaly and combination with other malformations (series of 16 patients)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Peters' anomaly associated with partial deletion of the long arm of chromosome 11.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Peters' anomaly in association with ring 21 chromosomal abnormality

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Brachymesomelia and Peters anomaly: a new syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Brief clinical report: corneal dermoids and short stature in brother and sister--a new syndrome?

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Three siblings with Peters' anomaly

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Peters' anomaly. The spectrum of associated ocular and systemic malformations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901120-6

10.1016/S0003-3995(02)01120-6

7 January 2021

Identifiers

DOI

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2 August 2017

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