(Q52184288)

26 April 2018

review article

1 reference

title

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

1 reference

26 April 2018

author name string

Zvulunov A

1

1 reference

26 April 2018

Kachko L

2

1 reference

26 April 2018

Manor E

3

1 reference

26 April 2018

Shinwell E

4

1 reference

26 April 2018

Carmi R

5

1 reference

26 April 2018

language of work or name

English

0 references

publication date

1 June 1998

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26 April 2018

British Journal of Dermatology

published in

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26 April 2018

volume

138

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26 April 2018

issue

6

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26 April 2018

page(s)

1046-1052

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26 April 2018

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

cites work

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Aplasia cutis congenita: a clinical review and proposal for classification

21 January 2018

1 reference

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

Fluorescence in situ hybridization

21 January 2018

1 reference

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

Focal dermal hypoplasia (Goltz syndrome).

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

10.1046/J.1365-2133.1998.02277.X

21 January 2018

Identifiers

DOI

1 reference

26 April 2018

PubMed ID

9747372

1 reference

26 April 2018