213 related articles for article (PubMed ID: 2667350)
1. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
Thomas IT; Frias JL; Cantu ES; Lafer CZ; Flannery DB; Graham JG
Am J Hum Genet; 1989 Aug; 45(2):193-205. PubMed ID: 2667350
[TBL] [Abstract][Full Text] [Related]
2. Hypomelanosis of Ito: a description, not a diagnosis.
Sybert VP
J Invest Dermatol; 1994 Nov; 103(5 Suppl):141S-143S. PubMed ID: 7963677
[TBL] [Abstract][Full Text] [Related]
3. Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.
Sybert VP; Pagon RA; Donlan M; Bradley CM
J Pediatr; 1990 Apr; 116(4):581-6. PubMed ID: 2319405
[TBL] [Abstract][Full Text] [Related]
4. Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.
Pavone V; Signorelli SS; Praticò AD; Corsello G; Savasta S; Falsaperla R; Pavone P; Sessa G; Ruggieri M
Medicine (Baltimore); 2016 Mar; 95(10):e2705. PubMed ID: 26962770
[TBL] [Abstract][Full Text] [Related]
5. Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases.
Ohashi H; Tsukahara M; Murano I; Naritomi K; Nishioka K; Miyake S; Kajii T
Am J Med Genet; 1992 Jul; 43(4):716-21. PubMed ID: 1621763
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 1952789
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 3236362
[TBL] [Abstract][Full Text] [Related]
8. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
Happle R
Am J Hum Genet; 1991 May; 48(5):1013-4. PubMed ID: 2018034
[No Abstract] [Full Text] [Related]
9. Pigmentary mosaicism of the hyperpigmented type in two half-brothers.
Horn D; Happle R; Neitzel H; Kunze J
Am J Med Genet; 2002 Sep; 112(1):65-9. PubMed ID: 12239723
[TBL] [Abstract][Full Text] [Related]
10. An unusual human mosaic for skin pigmentation.
Stoll C; Alembik Y; Grosshans E; de Saint Martin A
Genet Couns; 2002; 13(3):281-7. PubMed ID: 12416635
[TBL] [Abstract][Full Text] [Related]
11. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
Read AP; Donnai D
Am J Hum Genet; 1990 Jul; 47(1):166-8. PubMed ID: 2349946
[No Abstract] [Full Text] [Related]
12. 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. PubMed ID: 3464561
[TBL] [Abstract][Full Text] [Related]
13. Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism.
Küster W; König A
Am J Med Genet; 1999 Aug; 85(4):346-50. PubMed ID: 10398257
[TBL] [Abstract][Full Text] [Related]
14. [Trisomy 20 mosaicism revealed by pigmentary mosaicism of the Ito-type].
Girard C; Guillot B; Rivier F; Dalla Vale F; Bessis D
Ann Dermatol Venereol; 2005 Feb; 132(2):151-3. PubMed ID: 15798568
[TBL] [Abstract][Full Text] [Related]
15. [Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].
Ronger S; Till M; Kanitakis J; Balme B; Thomas L
Ann Dermatol Venereol; 2003 Nov; 130(11):1033-8. PubMed ID: 14724538
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 9856488
[TBL] [Abstract][Full Text] [Related]
17. Mosaic trisomy 7 in a patient with pigmentary abnormalities.
Verghese S; Newlin A; Miller M; Burton BK
Am J Med Genet; 1999 Dec; 87(5):371-4. PubMed ID: 10594873
[TBL] [Abstract][Full Text] [Related]
18. 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; 43(1):39-43. PubMed ID: 10818220
[TBL] [Abstract][Full Text] [Related]
19. Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.
Cantú ES; Thomas IT; Frias JL
Clin Genet; 1989 Sep; 36(3):189-95. PubMed ID: 2676269
[TBL] [Abstract][Full Text] [Related]
20. Hypomelanosis of ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10), +13/46,xy].
Yakinci C; Kutlu NO; Alp MN; Senol M; Durmaz Y; Budak T
Turk J Pediatr; 2002; 44(2):152-5. PubMed ID: 12026206
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]