Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism (Q33922438)

30 July 2017

title

Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism (English)

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30 July 2017

Tunca Y

1

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30 July 2017

Wilroy RS

2

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30 July 2017

Kadandale JS

3

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30 July 2017

Martens PR

4

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30 July 2017

Gunther WM

5

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30 July 2017

Tharapel AT

6

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30 July 2017

publication date

1 January 2000

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30 July 2017

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30 July 2017

volume

43

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30 July 2017

issue

1

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30 July 2017

page(s)

39-43

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Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Natural history of mosaic trisomy 14 syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Chromosome mosaicism in hypomelanosis of Ito.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

The gene for incontinentia pigmenti is assigned to Xq28.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2900012-5

10.1016/S0003-3995(00)00012-5

7 January 2021

Identifiers

DOI

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30 July 2017

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