341 related articles for article (PubMed ID: 11056419)
1. Phylloid hypomelanosis is closely related to mosaic trisomy 13.
Happle R
Eur J Dermatol; 2000; 10(7):511-2. PubMed ID: 11056419
[TBL] [Abstract][Full Text] [Related]
2. Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.
González-Enseñat MA; Vicente A; Poo P; Catalá V; Mar Pérez-Iribarne M; Fuster C; Geán E; Happle R
Arch Dermatol; 2009 May; 145(5):576-8. PubMed ID: 19451503
[TBL] [Abstract][Full Text] [Related]
3. Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis.
Faletra F; Berti I; Tommasini A; Pecile V; Cleva L; Alberini E; Bruno I; Gasparini P
Dermatology; 2012; 225(4):294-7. PubMed ID: 23095783
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Phylloid pattern of pigmentary disturbance in a case of complex mosaicism.
Ribeiro Noce T; de Pina-Neto JM; Happle R
Am J Med Genet; 2001 Jan; 98(2):145-7. PubMed ID: 11223850
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocutaneous syndrome].
Happle R
Hautarzt; 2001 Jan; 52(1):3-5. PubMed ID: 11220235
[TBL] [Abstract][Full Text] [Related]
8. Phylloid pigmentary pattern with mosaic trisomy 13.
Horn D; Rommeck M; Sommer D; Körner H
Pediatr Dermatol; 1997; 14(4):278-80. PubMed ID: 9263307
[TBL] [Abstract][Full Text] [Related]
9. Mosaic tetrasomy 13q and phylloid hypomelanosis: a case report and review of the literature.
Myers JN; Davis L; Sheehan D; Kulharya AS
Pediatr Dermatol; 2015; 32(2):263-6. PubMed ID: 24920397
[TBL] [Abstract][Full Text] [Related]
10. Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty.
Dhar SU; Robbins-Furman P; Levy ML; Patel A; Scaglia F
Am J Med Genet A; 2009 May; 149A(5):993-6. PubMed ID: 19334087
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis and genetic counseling for mosaic trisomy 13.
Chen CP
Taiwan J Obstet Gynecol; 2010 Mar; 49(1):13-22. PubMed ID: 20466287
[TBL] [Abstract][Full Text] [Related]
12. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes.
Taibjee SM; Hall D; Balderson D; Larkins S; Stubbs T; Moss C
Clin Exp Dermatol; 2009 Oct; 34(7):823-9. PubMed ID: 19438553
[TBL] [Abstract][Full Text] [Related]
13. The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights.
Forconi R; Bigoni S; Pacetti L; Host C; Schettini N; Zedde P; Buldrini B; Ferlini A; Bettoli V
Pediatr Dermatol; 2021 May; 38(3):637-639. PubMed ID: 33715178
[TBL] [Abstract][Full Text] [Related]
14. Phylloid hypomelanosis associated with a mosaic trisomy 13 in the 13q31.3-qter region: atypical phylloid distribution and typical hypomelanosis.
Oiso N; Sakai K; Nishio K; Kawada A
Pigment Cell Melanoma Res; 2017 Mar; 30(2):269-272. PubMed ID: 27930866
[No Abstract] [Full Text] [Related]
15. 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]
16. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
Crowe CA; Schwartz S; Black CJ; Jaswaney V
Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
[TBL] [Abstract][Full Text] [Related]
17. New association between ring chromosome 20 syndrome and hypomelanosis of Ito.
Cappanera S; Passamonti C; Zamponi N
Pediatr Neurol; 2011 Nov; 45(5):341-3. PubMed ID: 22000318
[TBL] [Abstract][Full Text] [Related]
18. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
Fogu G; Maserati E; Cambosu F; Moro MA; Poddie F; Soro G; Bandiera P; Serra G; Tusacciu G; Sanna G; Mazzarello V; Montella A
Eur J Med Genet; 2008; 51(4):303-14. PubMed ID: 18495567
[TBL] [Abstract][Full Text] [Related]
19. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
[TBL] [Abstract][Full Text] [Related]
20. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
