These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 14939114)

  • 21. SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies.
    Mauri L; Barone L; Al Oum M; Del Longo A; Piozzi E; Manfredini E; Stanzial F; Benedicenti F; Penco S; Patrosso MC
    Gene; 2014 Jan; 533(1):398-402. PubMed ID: 24096233
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Poliosis circumscripta: overview and underlying causes.
    Sleiman R; Kurban M; Succaria F; Abbas O
    J Am Acad Dermatol; 2013 Oct; 69(4):625-33. PubMed ID: 23850259
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Biology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa.
    Manga P; Kerr R; Ramsay M; Kromberg JG
    S Afr Med J; 2013 Jul; 103(12 Suppl 1):984-8. PubMed ID: 24300644
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Partial familial albinism (piebaldism): ultrastructural study].
    Grupper C; Pruniéras M; Hincky M; Garelly E
    Ann Dermatol Syphiligr (Paris); 1970; 97(3):267-86. PubMed ID: 5455226
    [No Abstract]   [Full Text] [Related]  

  • 25. ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM.
    BREATHNACH AS; FITZPATRICK TB; WYLLIE LM
    J Invest Dermatol; 1965 Jul; 45():28-37. PubMed ID: 14310308
    [No Abstract]   [Full Text] [Related]  

  • 26. Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis.
    Batrani M; Thole A; Kubba A; Mahajan K
    J Cutan Pathol; 2018 Dec; 45(12):918-922. PubMed ID: 30129079
    [TBL] [Abstract][Full Text] [Related]  

  • 27. "White forelock"-an embarassing curiosity.
    Philip J; Antony ; Joseph PP
    J Assoc Physicians India; 1981 Jun; 29(6):499-501. PubMed ID: 7320008
    [No Abstract]   [Full Text] [Related]  

  • 28. [Genetics of oculocutaneous albinism].
    Zühlke C; Stell A; Käsmann-Kellner B
    Ophthalmologe; 2007 Aug; 104(8):674-80. PubMed ID: 17646993
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Oculocutaneous and ocular albinism].
    Kubasch AS; Meurer M
    Hautarzt; 2017 Nov; 68(11):867-875. PubMed ID: 29018889
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Piebaldism].
    Küster W
    Hautarzt; 1987 Aug; 38(8):481-3. PubMed ID: 3654219
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.
    King RA; Townsend D; Oetting W; Summers CG; Olds DP; White JG; Spritz RA
    J Clin Invest; 1991 Mar; 87(3):1046-53. PubMed ID: 1900307
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutation analysis in a family with oculocutaneous albinism manifesting in the same generation of three branches.
    Preising MN; Forster H; Tan H; Lorenz B; de Jong PT; Plomp AS
    Mol Vis; 2007 Oct; 13():1851-5. PubMed ID: 17960121
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era.
    Gaudiello F; Ferrillo M; Vastarella M; Fabbrocini G; Patrì A
    Skin Appendage Disord; 2021 Feb; 7(2):120-122. PubMed ID: 33791342
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mice transgenic for Kit(V620A): recapitulation of piebaldism but not progressive depigmentation seen in humans with this mutation.
    Tosaki H; Kunisada T; Motohashi T; Aoki H; Yoshida H; Kitajima Y
    J Invest Dermatol; 2006 May; 126(5):1111-8. PubMed ID: 16456533
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Variable expression of vision in sibs with albinism.
    Summers CG; Creel D; Townsend D; King RA
    Am J Med Genet; 1991 Sep; 40(3):327-31. PubMed ID: 1951438
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Squamous-cell carcinoma in situ in a patient with oculocutaneous albinism.
    Berger E; Hunt R; Tzu J; Patel R; Sanchez M
    Dermatol Online J; 2011 Oct; 17(10):22. PubMed ID: 22031648
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Piebaldism.
    Oiso N; Fukai K; Kawada A; Suzuki T
    J Dermatol; 2013 May; 40(5):330-5. PubMed ID: 22670867
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Waardenburg Syndrome type 1: A case report.
    Demirci GT; Atıs G; Altunay IK
    Dermatol Online J; 2011 Nov; 17(11):3. PubMed ID: 22136859
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Technical advances in prenatal diagnosis of tyrosinase-negative oculocutaneous albinism.
    Shimizu H
    Acta Derm Venereol; 1997 Jan; 77(1):10-3. PubMed ID: 9059668
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].
    COUTEAU-LAGARDE JM; COLLIER M
    J Genet Hum; 1963 Dec; 12():146-53. PubMed ID: 14136826
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.