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Links from PubMed

Items: 8

1.

Letter: Half chromatid mutations may explain incontinentia pigmenti in males.

Lenz W.

Am J Hum Genet. 1975 Sep;27(5):690-1. No abstract available.

2.

Chromosomal instability in incontinentia pigmenti: study of four families.

Pallotta R, Dalprá L.

Ann Genet. 1988;31(1):27-31. Review.

PMID:
3281567
3.

Hypomelanosis of Ito (incontinentia pigmenti achromians).

Gordon N.

Dev Med Child Neurol. 1994 Mar;36(3):271-4. Review. No abstract available.

PMID:
7511121
4.

Genetic counselling in hypomelanosis of Ito: case report and review.

Moss C, Burn J.

Clin Genet. 1988 Aug;34(2):109-15. Review.

PMID:
3056640
5.

Dominant disorders with multiple organ involvement.

Kegel MF.

Dermatol Clin. 1987 Jan;5(1):205-19. Review.

PMID:
3549076
6.

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

Koiffmann CP, de Souza DH, Diament A, Ventura HB, Alves RS, Kihara S, Wajntal A.

Am J Med Genet. 1993 Jun 15;46(5):529-33. Review.

PMID:
8322815
7.

Pigmentary abnormalities in genetic disorders.

Lucky AW.

Dermatol Clin. 1988 Apr;6(2):193-203. Review.

PMID:
3132341
8.

Incontinentia pigmenti, a chromosomal instability syndrome, is associated with childhood malignancy.

Roberts WM, Jenkins JJ, Moorhead EL 2nd, Douglass EC.

Cancer. 1988 Dec 1;62(11):2370-2. Review.

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