Cuscó I, del Campo M, Vilardell M, González E, Gener B, Galán E, Toledo L, Pérez-Jurado LA. Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration. „BMC Med Genet”. 9, s. 27, 2008. DOI: 10.1186/1471-2350-9-27. PMID: 18405349.
Shah M, Bogucki B, Mavers M, deMello DE, Knutsen A. Cardiac conduction abnormalities and congenital immunodeficiency in a child with Kabuki syndrome: case report. „BMC Med Genet”. Jul 25;6, s. 28, 2005. DOI: 10.1186/1471-2350-6-28. PMID: 16042804.
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Cuscó I, del Campo M, Vilardell M, González E, Gener B, Galán E, Toledo L, Pérez-Jurado LA. Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration. „BMC Med Genet”. 9, s. 27, 2008. DOI: 10.1186/1471-2350-9-27. PMID: 18405349.
Shah M, Bogucki B, Mavers M, deMello DE, Knutsen A. Cardiac conduction abnormalities and congenital immunodeficiency in a child with Kabuki syndrome: case report. „BMC Med Genet”. Jul 25;6, s. 28, 2005. DOI: 10.1186/1471-2350-6-28. PMID: 16042804.
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Kuroki Y, Suzuki Y, Chyo H, Hata A, Matsui I. A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip and skeletal anomalies associated with postnatal dwarfism and mental retardation. „J Pediatr”. 99. 4, s. 570–573, 1981. PMID: 7277097.
Niikawa N, Kuroki Y, Kajii T, Matsuura N, Ishikiriyama S, Tonoki H, Ishikawa N, Yamada Y, Fujita M, Umemoto H, et al. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients. „Am J Med Genet”. 31. 3, s. 565–589, 1988. PMID: 3067577.
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