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8. Anesthesia management in Kabuki make-up syndrome. Sivaci R; Kahveci OK; Celik M; Altuntas A; Solak M Saudi Med J; 2005 Dec; 26(12):1980-2. PubMed ID: 16380786 [TBL] [Abstract][Full Text] [Related]
9. Kabuki make-up syndrome: a review. Matsumoto N; Niikawa N Am J Med Genet C Semin Med Genet; 2003 Feb; 117C(1):57-65. PubMed ID: 12561059 [TBL] [Abstract][Full Text] [Related]
10. Inheritance in Kabuki make-up (Niikawa-Kuroki) syndrome. Kobayashi O; Sakuragawa N Am J Med Genet; 1996 Jan; 61(1):92-3. PubMed ID: 8741928 [No 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]
13. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2. Li M; Zackai EH; Niikawa N; Kaplan P; Driscoll DA Am J Med Genet; 1996 Oct; 65(2):101-3. PubMed ID: 8911598 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. The spectrum of congenital cardiac malformations encountered in six children with Kabuki syndrome. McMahon CJ; Reardon W Cardiol Young; 2006 Feb; 16(1):30-3. PubMed ID: 16454874 [TBL] [Abstract][Full Text] [Related]
16. 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]
19. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents. Stoll C; Alembik Y; Lutz P Genet Couns; 1994; 5(2):161-5. PubMed ID: 7917125 [TBL] [Abstract][Full Text] [Related]
20. The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients. Schrander-Stumpel C; Meinecke P; Wilson G; Gillessen-Kaesbach G; Tinschert S; König R; Philip N; Rizzo R; Schrander J; Pfeiffer L Eur J Pediatr; 1994 Jun; 153(6):438-45. PubMed ID: 8088300 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]