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Items: 1 to 20 of 127

1.

Hypomelanosis of Ito: spectrum of the disease.

Glover MT, Brett EM, Atherton DJ.

J Pediatr. 1989 Jul;115(1):75-80.

PMID:
2738798
2.

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

Donnai D, Read AP, McKeown C, Andrews T.

J Med Genet. 1988 Dec;25(12):809-18.

3.
4.

EEG findings in hypomelanosis of Ito.

Esquivel EE, Pitt MC, Boyd SG.

Neuropediatrics. 1991 Nov;22(4):216-9.

PMID:
1775218
5.

Hypomelanosis of Ito: a description, not a diagnosis.

Sybert VP.

J Invest Dermatol. 1994 Nov;103(5 Suppl):141S-143S. Review.

PMID:
7963677
6.

Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp.

Fritz B, Küster W, Orstavik KH, Naumova A, Spranger J, Rehder H.

Hum Genet. 1998 Oct;103(4):441-9. Review.

PMID:
9856488
7.

Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome.

Lenzini E, Bertoli P, Artifoni L, Battistella PA, Baccichetti C, Peserico A.

Ann Genet. 1991;34(1):30-2. Review.

PMID:
1952789
8.

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
9.

Chromosome mosaicism in hypomelanosis of Ito.

Ritter CL, Steele MW, Wenger SL, Cohen BA.

Am J Med Genet. 1990 Jan;35(1):14-7.

PMID:
2301465
10.

Hypomelanosis of Ito--a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicism.

Chitayat D, Friedman JM, Johnston MM.

Am J Med Genet. 1990 Mar;35(3):422-4.

PMID:
2309792
11.
12.

Abnormal head MRI in a neurologically normal boy with hypomelanosis of Ito.

Fryburg JS, Lin KY, Matsumoto J.

Am J Med Genet. 1996 Dec 11;66(2):200-3.

PMID:
8958331
13.

Hypomelanosis of Ito (incontinentia pigmenti achromians). Ophthalmological evidence for somatic mosaicism.

Rott HD, Lang GE, Huk W, Pfeiffer RA.

Ophthalmic Paediatr Genet. 1990 Dec;11(4):273-9.

PMID:
2096355
14.

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Thomas IT, Frias JL, Cantu ES, Lafer CZ, Flannery DB, Graham JG Jr.

Am J Hum Genet. 1989 Aug;45(2):193-205. Review.

15.

Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.

Bocian E, Mazurczak T, Buława E, Stańczak H, Rowicka G.

J Med Genet. 1993 Jul;30(7):614-5.

16.

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

Tunca Y, Wilroy RS, Kadandale JS, Martens PR, Gunther WM, Tharapel AT.

Ann Genet. 2000 Jan-Mar;43(1):39-43.

PMID:
10818220
17.

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

Turleau C, Taillard F, Doussau de Bazignan M, Delépine N, Desbois JC, de Grouchy J.

Hum Genet. 1986 Oct;74(2):185-7.

PMID:
3464561
18.

Epidermal mosaicism and Blaschko's lines.

Moss C, Larkins S, Stacey M, Blight A, Farndon PA, Davison EV.

J Med Genet. 1993 Sep;30(9):752-5.

19.

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
20.

Hemifacial hypoplasia and hypomelanosis of Ito.

Tan ST, Slaney SF, Ashworth G, Poole MD.

J Craniomaxillofac Surg. 1995 Oct;23(5):274-9.

PMID:
8530701
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