BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

327 related articles for article (PubMed ID: 10594873)

  • 1. 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]  

  • 2. 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. PubMed ID: 2309792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
    Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Linear and whorled hypermelanosis.
    Di Lernia V
    Pediatr Dermatol; 2007; 24(3):205-10. PubMed ID: 17542865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.
    Taibjee SM; Bennett DC; Moss C
    Br J Dermatol; 2004 Aug; 151(2):269-82. PubMed ID: 15327534
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linear hypopigmentation and hyperpigmentation, including mosaicism.
    Loomis CA
    Semin Cutan Med Surg; 1997 Mar; 16(1):44-53. PubMed ID: 9125765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 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. The clinical profile of children in India with pigmentary anomalies along the lines of Blaschko and central nervous system manifestations.
    Pinheiro A; Mathew MC; Thomas M; Jacob M; Srivastava VM; Cherian R; Raju R; George R
    Pediatr Dermatol; 2007; 24(1):11-7. PubMed ID: 17300642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [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]  

  • 15. 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]  

  • 16. Blaschkolinear skin pigmentary variation due to trisomy 7 mosaicism.
    Kayser M; Henderson LB; Kreutzman J; Schreck R; Graham JM
    Am J Med Genet; 2000 Nov; 95(3):281-4. PubMed ID: 11102936
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism.
    Magenis E; Webb MJ; Spears B; Opitz JM
    Am J Med Genet; 1999 Dec; 87(5):375-83. PubMed ID: 10594874
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 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]
    of 17.