X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp.

Author:

Hatchwell E,Robinson D,Crolla J A,Cockwell A E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Incontinentia pigmenti achromians. A singular case of nevus depigmentosus systematicus bilateralis;Ito, M.;Tohoku 7 Exp Med (Sendai)

2. Hypomelanosis of Ito: a manifestation of mosaicism or chimerism;Donnai D, Read AP, McKeown C, Andrews T;_J Med Genet,1988

3. Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito;Sybert, V.P.; Pagon, R.A.; Donlan, M.; Bradley, C.M.;J Pediatr,1990

4. Incontinentia pigmenti (type 1) and X; 5 translocation;Bitoun, P.; Philippe, C.; Cherif, M.; Mulcahy, M.T.; Gilgenkrantz, S.;Ann Genet (Paris),1992

5. Incontinentia pigmenti achromians (hypomelanosis of Ito, MIM 146150): further evidence of localization at Xpll;Koiffmann, C.P.; De, S.D.; Diament, A.;Am 7 Med Genet,1993

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2. INCONTINENTIA PIGMENTI;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

3. Incontinentia Pigmenti;Harper's Textbook of Pediatric Dermatology;2019-11-20

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5. Hypomelanosis of Ito;Atlas of Genetic Diagnosis and Counseling;2017

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