(Q33594861)

28 July 2017

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title

Incontinentia pigmenti (Bloch-Sulzberger syndrome). (English)

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28 July 2017

Landy SJ

1

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28 July 2017

Donnai D

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 January 1993

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

30

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28 July 2017

issue

1

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28 July 2017

page(s)

53-59

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Ocular lesions in incontinentia pigmenti.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Painful subungual keratotic tumors in incontinentia pigmenti.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritance

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti in a boy with Klinefelter's syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti: the development of pseudoglioma

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

The gene for incontinentia pigmenti is assigned to Xq28.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Selection against lethal alleles in females heterozygous for incontinentia pigmenti

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Early diagnosis of the retinopathy of incontinentia pigmenti: successful treatment by cryotherapy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Chromosome mosaicism in hypomelanosis of Ito.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti. A world statistical analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Letter: Half chromatid mutations may explain incontinentia pigmenti in males

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Half chromatid mutations: transmission in humans?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016235

Incontinentia pigmenti associated with subungual tumors

14 July 2018

1 reference

12 December 2020

[Painful and spontaneously healing subungual dyskeratotic tumors; their relation to incontinentia pigmenti]

1 reference

12 December 2020

Depigmented lesions in incontinentia pigmenti. A useful diagnostic sign

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12 December 2020

Incontinentia pigmenti

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12 December 2020

Incontinentia pigmenti. A four-generation study

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12 December 2020

Anhidrotic and achromians lesions in incontinentia pigmenti

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12 December 2020

Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation

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12 December 2020

Incontinentia pigmenti

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12 December 2020

Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11

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12 December 2020

Incontinentia pigmenti: XXY male with a family history

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12 December 2020

The characteristic dentition of incontinentia pigmenti

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12 December 2020

Incontinentia pigmenti. A longitudinal study

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12 December 2020

Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?

1 reference

12 December 2020

Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma

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12 December 2020

Diploid/triploid mixoploidy and hypomelanosis of Ito

1 reference

12 December 2020

Incontinentia pigmenti: eosinophil chemotactic activity of the crusted scales in the vesiculobullous stage

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12 December 2020

Subungual tumors in incontinentia pigmenti

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12 December 2020

Tentative assignment of hypomelanosis of Ito to 9q33----qter

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12 December 2020

Incontinentia pigmenti (Bloch-Sulzberger syndrome). A report of four additional cases

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12 December 2020

Identifiers

DOI

10.1136/JMG.30.1.53

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28 July 2017

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28 July 2017

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