Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22. (Q52184288)

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scientific article published in June 1998

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English	Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22.	scientific article published in June 1998

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Europe PubMed Central

PubMed publication ID

9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

review article

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Europe PubMed Central

title

Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22. (English)

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Europe PubMed Central

PubMed publication ID

9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

author name string

Zvulunov A

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1

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9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

Kachko L

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2

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9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

Manor E

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3

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PubMed publication ID

9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

Shinwell E

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4

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9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

Carmi R

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5

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9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

language of work or name

English

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publication date

1 June 1998

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9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

published in

British Journal of Dermatology

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PubMed publication ID

9747372

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26 April 2018

reference URL

http://europepmc.org/abstract/MED/9747372

volume

138

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PubMed publication ID

9747372

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26 April 2018

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http://europepmc.org/abstract/MED/9747372

issue

6

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PubMed publication ID

9747372

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26 April 2018

reference URL

http://europepmc.org/abstract/MED/9747372

page(s)

1046-1052

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9747372

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26 April 2018

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cites work

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Xp microdeletion syndrome characterized by pathognomonic linear skin defects on the head and neck

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Aplasia cutis congenita: a clinical review and proposal for classification

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Fluorescence in situ hybridization

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Focal dermal hypoplasia (Goltz syndrome).

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Microphthalmia and chorioretinal lesions in a girl with an Xp22.2-pter deletion and partial 3p trisomy: clinical observations relevant to Aicardi syndrome gene localization

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1365-2133.1998.02277.X

retrieved

21 January 2018

Identifiers

DOI

10.1046/J.1365-2133.1998.02277.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9747372

retrieved

26 April 2018

reference URL

http://europepmc.org/abstract/MED/9747372

PubMed publication ID

9747372

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9747372

retrieved

26 April 2018

reference URL

http://europepmc.org/abstract/MED/9747372

 

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