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 *

201 related articles for article (PubMed ID: 8298741)

  • 1. Kabuki make-up syndrome and hearing impairment.
    Say B; McCutcheon L; Todd C; Hough JV
    Clin Dysmorphol; 1993 Jan; 2(1):68-70. PubMed ID: 8298741
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kabuki syndrome: a review.
    Adam MP; Hudgins L
    Clin Genet; 2005 Mar; 67(3):209-19. PubMed ID: 15691356
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
    Niikawa N; Kuroki Y; Kajii T; Matsuura N; Ishikiriyama S; Tonoki H; Ishikawa N; Yamada Y; Fujita M; Umemoto H
    Am J Med Genet; 1988 Nov; 31(3):565-89. PubMed ID: 3067577
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression.
    Su PH; Kuo PL; Chen SJ; Chen JY; Yu JS; Liu YL; Kao IW
    Acta Paediatr Taiwan; 2007; 48(1):28-31. PubMed ID: 19653414
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Niikawa-Kuroki syndrome (the so-called Kabuki make up syndrome)].
    Braun OH; Schmid E
    Klin Padiatr; 1986; 198(1):65-8. PubMed ID: 3959492
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases.
    Philip N; Meinecke P; David A; Dean J; Ayme S; Clark R; Gross-Kieselstein E; Hosenfeld D; Moncla A; Muller D
    Clin Dysmorphol; 1992 Apr; 1(2):63-77. PubMed ID: 1285376
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cutis laxa in Kabuki make-up syndrome.
    Vaccaro M; Salpietro DC; Briuglia S; Merlino MV; Guarneri F; Dallapiccola B
    J Am Acad Dermatol; 2005 Nov; 53(5 Suppl 1):S247-51. PubMed ID: 16227101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deafness and Mondini dysplasia in Kabuki (Niikawa-Kuroki) syndrome. Report of a case and review of the literature.
    Toutain A; Plée Y; Ployet MJ; Benoit S; Perrot A; Sembely C; Barthez MA; Moraine C
    Genet Couns; 1997; 8(2):99-105. PubMed ID: 9219007
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Kabuki syndrome].
    Stankovics J
    Orv Hetil; 1995 Aug; 136(34):1841-3. PubMed ID: 7651720
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Kabuki make-up syndrome with unilateral renal agenesis.
    Rosti RO; Kayserili H
    Turk J Pediatr; 2009; 51(3):298-300. PubMed ID: 19817278
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.
    Halal F; Gledhill R; Dudkiewicz A
    Am J Med Genet; 1989 Jul; 33(3):376-81. PubMed ID: 2801772
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A case report of Kabuki make-up syndrome with cytomegalovirus infection.
    Kashiwagi Y; Numabe H; Kawashima H; Mori M; Miyajima T; Tsuyuki K; Takekuma K; Hoshika A
    J Infect; 2004 Apr; 48(3):278-82. PubMed ID: 15001308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
    Galán-Gómez E; Cardesa-García JJ; Campo-Sampedro FM; Salamanca-Maesso C; Martínez-Frías ML; Frías JL
    Am J Med Genet; 1995 Nov; 59(3):276-82. PubMed ID: 8599349
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Niikawa-Kuroki (Kabuki) syndrome and hearing impairment].
    Lüerssen K; Ptok M
    HNO; 2004 May; 52(5):451-4. PubMed ID: 15138652
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
    Stoll C; Terzic J; Fischbach M
    Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The craniodigital syndrome of Scott: report of a second family.
    Lorenz P; Hinkel GK; Hoffmann C; Rupprecht E
    Am J Med Genet; 1990 Oct; 37(2):224-6. PubMed ID: 2174209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome).
    Anandan M; Porter NJ; Nemeth AH; Blair E; Downes SM
    Ophthalmic Genet; 2005 Dec; 26(4):181-3. PubMed ID: 16352479
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
    Simosa V; Penchaszadeh VB; Bustos T
    Am J Med Genet; 1989 Feb; 32(2):184-6. PubMed ID: 2929657
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y; Kajii T
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndrome.
    Franceschini P; Vardeu MP; Guala A; Franceschini D; Testa A; Corrias A; Chiabotto P
    Am J Med Genet; 1993 Sep; 47(3):423-5. PubMed ID: 8135293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.