PubMed for id: 336799

Year	Number of Results
1977	1
1981	3
1990	1
1993	1
1997	1
1999	1
2002	1
2004	1
2005	1
2008	1
2011	1
2012	1
2014	1
2015	1
2016	1
2018	2
2019	2
2020	2
2022	1
2024	0

1

Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.

Yu CW, Chen H, Baucum RW, Hand AM. Yu CW, et al. Ann Genet. 1981;24(3):158-61. Ann Genet. 1981. PMID: 6974525

2

Anesthesia management in a patient with kabuki syndrome.

Atalay YO, Kaya C, Ustun YB, Sahinoglu AH. Atalay YO, et al. Med Arch. 2014 Oct;68(5):359-60. doi: 10.5455/medarh.2014.68.359-360. Epub 2014 Oct 15. Med Arch. 2014. PMID: 25568573 Free PMC article.

3

Oral features in Kabuki make-up Syndrome.

Spano G, Campus G, Bortone A, Lai V, Lugliè PF. Spano G, et al. Eur J Paediatr Dent. 2008 Sep;9(3):149-52. Eur J Paediatr Dent. 2008. PMID: 18844445

4

Midline skeletodental morphology in holoprosencephaly.

Kjaer I, Keeling JW, Fischer Hansen B, Becktor KB. Kjaer I, et al. Cleft Palate Craniofac J. 2002 May;39(3):357-63. doi: 10.1597/1545-1569_2002_039_0357_msmih_2.0.co_2. Cleft Palate Craniofac J. 2002. PMID: 12019014

5

A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation.

Kuroki Y, Suzuki Y, Chyo H, Hata A, Matsui I. Kuroki Y, et al. J Pediatr. 1981 Oct;99(4):570-3. doi: 10.1016/s0022-3476(81)80256-9. J Pediatr. 1981. PMID: 7277097

6

Brief clinical report: the del(4) (q31) syndrome- a recognizable disorder with atypical Robin malformation sequence.

Davis JM, Clarren SK, Salk DJ. Davis JM, et al. Am J Med Genet. 1981;9(2):113-7. doi: 10.1002/ajmg.1320090205. Am J Med Genet. 1981. PMID: 7258224

7

EVEN-PLUS syndrome: A case report with novel variants in HSPA9 and evidence of HSPA9 gene dysfunction.

Younger G, Vetrini F, Weaver DD, Lynnes TC, Treat K, Pratt VM, Torres-Martinez W. Younger G, et al. Am J Med Genet A. 2020 Nov;182(11):2501-2507. doi: 10.1002/ajmg.a.61808. Epub 2020 Sep 1. Am J Med Genet A. 2020. PMID: 32869452

8

A novel mutation in the ZNF462 gene c.3306dup; p.(Gln1103Thrfs*10) is associated to Weiss-Kruszka syndrome. A case report.

González-Tarancón R, Salvador-Rupérez E, Miramar Gallart MD, Barroso E, Díez García-Prieto I, Pérez Delgado R, López Pisón J, García Jiménez MC. González-Tarancón R, et al. Acta Clin Belg. 2022 Feb;77(1):118-121. doi: 10.1080/17843286.2020.1780391. Epub 2020 Jun 16. Acta Clin Belg. 2022. PMID: 32543299

9

Evaluation of Polycaprolactone-Associated Human Nasal Chondrocytes as a Therapeutic Agent for Cartilage Repair.

Kim DH, Lim MH, Jeun JH, Park SH, Lee W, Park SH, Kwon MY, Hwang SH, Kim SW. Kim DH, et al. Tissue Eng Regen Med. 2019 Aug 19;16(6):605-614. doi: 10.1007/s13770-019-00210-1. eCollection 2019 Dec. Tissue Eng Regen Med. 2019. PMID: 31824823 Free PMC article.

10

Nasal Elongation with Septal Half Extension Graft: Modification of Conventional Septal Extension Graft Using Minimal Septal Cartilage.

Lee SH, Lee HB, Kang ET. Lee SH, et al. Aesthetic Plast Surg. 2018 Dec;42(6):1648-1654. doi: 10.1007/s00266-018-1219-6. Epub 2018 Sep 14. Aesthetic Plast Surg. 2018. PMID: 30218153

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