Unceasing Efforts

(주)캔서롭은 끊임없는 연구개발과 정직한 기업정신으로
항상 최선을 다하는 최고의 분자진단 전문기업이 되겠습니다.

Home/News/Notices/논문

논문

  • *

    Array Comparative Genomic Hybridization as the First-line Investigation for Neonates with Congenital Heart Disease: Experience in a Single Tertiary Center.Korean Circ J. 2018 Mar;48(3):209-216

    원문보기
  • *

    A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.Clin Exp Reprod Med. 2014 Dec;41(4):168-73

    원문보기
  • *

    Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center.Obstet Gynecol Sci. 2018 Jan;61(1):95-101

    원문보기
  • *

    Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization.J Korean Med Sci. 2016 Aug;31(8):1307-18

    원문보기
  • *

    Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center study.Yonsei Med J. 2013 Nov;54(6):1463-70

    원문보기
  • *

    Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.Ann Clin Lab Sci. 2013 Summer;43(3):332-6

    원문보기
  • *

    Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH.J Genet Med. 2013 Jun;10(1):52-56

    원문보기
  • *

    Comprehensive chromosome analysis of blastocysts before implantation using array CGH.Mol Cytogenet. 2013 Jun 3;6(1):22

    원문보기
  • *

    The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns.Mol Cytogenet. 2013 Jun 1;6(1):21

    원문보기
  • *

    22q11.2 Microduplication with thyroid hemiagenesis.Horm Res Paediatr. 2013;79(4):243-9

    원문보기
  • *

    Reciprocal deletion and duplication of 17p11.2-11.2: Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome.J Korean Med Sci. 2012 Dec;27(12):1586-90

    원문보기
  • *

    Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.J Hum Genet. 2013 Feb;58(2):73-7

    원문보기
  • *

    Clinical and cytogenetic features of a Potocki-Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1.Brain Dev. 2013 Aug;35(7):681-5

    원문보기
  • *

    14q32.33 Deletion Identified by array-CGH in a 5-year old-girl with Seizure.J Genet Med. 2011 Jun;8(1):62-66

    원문보기
  • *

    Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.Mol Cytogenet. 2011 May 9;4:12

    원문보기
  • *

    Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.J Korean Med Sci. 2010 Dec;25(12):1798-801

    원문보기
  • *

    Clinical and genetic characteristics of Korean patients with Gaucher disease.Blood Cells Mol Dis. 2011 Jan 15;46(1):11-4

    원문보기
  • *

    Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis Type 1J Kor Med Sci, 2010 Feb;25:804-808

    원문보기
  • *

    The spectrum of 5p deletion in Korean 20 patients with Cri du chat syndrome.J Genet Med. 2007 Dec;4(2):133-141

    원문보기