- A Case with Balanced Chromosome Rearrangement Involving Chromosomes 9, 14, and 13 in a Woman with Recurrent Abortion
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Kim SK, Kim HJ, Yang YH, Kim IK, Bai SW, Kim JY, Park KH, Cho DJ, Song CH
- KMID: 720632
- Yonsei Med J.
- 2001 Jun;42(3):345-348.
- doi: 10.3349/ymj.2001.42.3.345
A phenotypically normal couple was referred for cytogenetic evaluation due to three consecutive first-trimester spontaneous abortions. Chromosomal analysis from peripheral blood was performed according to standard cytogenetic methods using G-banding... -
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- Loss of Heterozygosity on Chromosomes 3p,8p,9p and 17p in the Progression of Squamous Cell Carcinoma of the Larynx
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Yoo WJ, Cho SH, Lee YS, Park GS, Kim MS, Kim BK, Park WS, Lee JY, Kang CS
- KMID: 1786810
- J Korean Med Sci.
- 2004 Jun;19(3):345-351.
- doi: 10.3346/jkms.2004.19.3.345
Previous molecular genetic studies of laryngeal squamous cell carcinoma (SCC)have shown certain chromosomal regions with recurring alterations. But studies of sequential molecular alterations and genetic progression model of laryngeal SCC... -
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- A Case of Split Hand Split Foot Malformation Associated with Pericentric Inversion of Chromosome 9
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Ko HY, Kim TY, Park HJ, Lee KH, Choi EJ, Kim JK, Chung HL, Kim WT
- KMID: 2280588
- Korean J Perinatol.
- 2006 Sep;17(3):334-339.
Split hand split foot malformation (SHFM) is a human developmental disorder characterized by a deep median cleft in the hands and feet, missing digits, and fusion of the remaining digits.... -
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- Assignments of the tyrosinase related protein-1 and -2 genes to human chromosome bands 9p23 and 13q32.1 by in situ hybridization
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Lee YM, Ha MJ, Ryu MS, Moon E, Im S, Kim HJ, Kim W
- KMID: 711764
- Yonsei Med J.
- 2000 Jun;41(3):398-400.
- doi: 10.3349/ymj.2000.41.3.398
To determine the precise chromosomal localization of tyrosine related protein-1 and -2 (TRP-1 and TRP-2) genes by fluorescence in situ hybridization, we used DNAs isolated from human bacterial artificial chromosome... -
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- Microsatellite Alterations of Chromosome 9p, 13q, 16q in Hepatocellular Carcinoma
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Cho SJ, Kim NR, Min YK, Joh YG, Cho MY, Suh SO, Yeom BW, Won NH
- KMID: 2095938
- J Korean Surg Soc.
- 2001 Sep;61(3):305-311.
PURPOSE: Hepatocellular carcinoma (HCC) patients are asymptomatic and the tumor remains in an unresectable state until the tumor progresses. Recently much efforts for elucidation of the early hepatocarcinogenesis have been... -
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- Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
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Choi A, Oh JY, Kim M, Jang W, Jang DH
- KMID: 2440817
- Ann Rehabil Med.
- 2017 Oct;41(5):881-886.
- doi: 10.5535/arm.2017.41.5.881
Patients with a duplication from 7q36 to the terminus or a deletion of 9p24 have been reported, whereas those harboring both mutations have not. Here, we report a patient with... -
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- Loss of Heterozygosity on Chromosome 3p, 9p, 17p in Oral & Oropharyngeal Squamous Cell Carcinoma
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Lee SH, Kim MS, Sun DI, Song CJ, Cho SH
- KMID: 2274729
- Korean J Otolaryngol-Head Neck Surg.
- 2000 Jul;43(7):746-750.
BACKGROUND AND OBJECTIVES: Patients of oral and oropharyngeal squamous cell carcinoma in the comparable stage have diverse clinical courses and responses to similar treatment. Understanding the genetic alterations that occur... -
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- A Case of Partial Trisomy 9q Derived from Paternal Chromosome
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Jung JE, Song EJ, Park HJ, Lee KH, Lee KH, Choi EJ, Kim JK, Chung HL, Seo ES, Kim WT
- KMID: 2144509
- J Korean Soc Neonatol.
- 2009 May;16(1):71-75.
There are few cases of partial trisomy of 9q, known as partial 9q trisomy syndrome with low birth weight, microcephaly, hypotelorism, beaked nose, small lip, long finger, hypertrophic pyloric stenosis,... -
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- Cytogenetic Study in 535 Couples with Recurrent Spontaneous Abortions in Korea
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Hwang HS, Yang ES, Hong WK, Kim MS, Yang YH
- KMID: 2085169
- Korean J Fertil Steril.
- 2005 Jun;32(2):113-120.
OBJECTIVE: The purposes of this study were to investigate the types and the incidences of chromosomal abnormalities, and to provide an explanation for the genetic causations of recurrent spontaneous abortions... -
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- A Case of Partial Trisomy 9pter --> q13 due to Paternal Balanced Translocation t (9;21) (q13;q21)
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Woo KS, Kim KE, Kwon EY, Kim JP, Han JY
- KMID: 854855
- Korean J Lab Med.
- 2008 Apr;28(2):155-159.
- doi: 10.3343/kjlm.2008.28.2.155
Trisomy 9p is one of the most frequent autosomal anomalies compatible with a long survival rate. Clinical characteristics are craniofacial dysmorphisms including hypertelorism, prominent nose, deepset eyes, and down-slanting palpebral... -
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- Analysis of Breakpoints of bcr-abl Fusion Gene Using RT-PCR
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Shin S, Park SS, Cho HI, Hur M, Lee YJ
- KMID: 2031000
- Korean J Clin Pathol.
- 1999 Aug;19(4):369-374.
BACKGROUND: Three types of chimeric mRNA can be expressed as a result of fusion of abl gene on chromosome 9 and bcr gene on chromosome 22. These are b3a2, b2a2,... -
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- Isolated 9p Duplication With der(Y)t(Y;9)(q12;p13.2) in a Male Patient With Cardiac Defect and Mental Retardation Confirmed by Chromosomal Microarray
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Oh M, Cho IJ, Shin S, Lee ST, Choi JR
- KMID: 2373525
- Ann Lab Med.
- 2016 Mar;36(2):191-193.
- doi: 10.3343/alm.2016.36.2.191
No abstract available. -
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- A Case of Duplication 9q Syndrome
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Hwang MJ, Choi YY, Ma JS, Hwang TJ
- KMID: 1566099
- J Korean Soc Neonatol.
- 1998 Nov;5(2):193-197.
Since the first description of the trisomy 9p in 1970, over one hundred cases have been described with the advanced chromosomal banding technique. Clinical findings include growth and mental retardation... -
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- Incidence and Karyotypes According to Each Chromosome in 13 Cases with Inversion
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Chung SR
- KMID: 2072216
- Korean J Perinatol.
- 2009 Dec;20(4):361-369.
PURPOSE: This study was aimed to evaluate the incidence and karyotypes according to chromosome in 13 cases with inversion detected by cytogenetic analysis. METHODS: The incidence of inversion was calculated and... -
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- A Case of 9p-Syndrome due to a Balanced Maternal Translocation t(9;16) (p22;p13.2)
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Kim KH, Sin SD, Han JY, Kim JM, Shaffer LG
- KMID: 2089458
- Korean J Clin Pathol.
- 1997 Aug;17(4):676-680.
The deletion 9p syndrome is a well characterized syndrome with about one hundred cases having been reported. Most patients have dysmorphic facial features, cardiac anomalies, and mental retardation. We report... -
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- Cytogenetic abnormalities in patients with reproductive dysfunction
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Yun JS, Jang SK, Choi OH
- KMID: 2273132
- Korean J Obstet Gynecol.
- 2007 May;50(5):760-768.
OBJECTIVE: The aim of this study was to investigate the relationship between chromosome abnormalities and male or female reproductive dysfunction and to be convinced of the role of pericentric inversion... -
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- Deletions of 9p21 and TP53 in bladder cancer
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Park WS, Oh MJ, Lee HK, Lee KO, Rhyu MG, Dong SM, Lee JY, Kim SH
- KMID: 644955
- J Korean Med Sci.
- 1996 Jun;11(3):233-238.
- doi: 10.3346/jkms.1996.11.3.233
The objective of this study was to characterize the alterations of 9p21 and TP53 in Korean transitional bladder cancer and to assess the relationship between the histopathologic parameter and the... -
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- A Case of Partial Short Arm Deletion in Chromosome 9 with Inguinal Hernia, Testicular Cystic Lesion, and Arthrogryposis Multiplex Congenita
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Kim EJ, Chung SH, Park TS, Choi YS
- KMID: 2379660
- Neonatal Med.
- 2017 May;24(2):88-91.
- doi: 10.5385/nm.2017.24.2.88
Chromosome 9p syndrome is a rare chromosomal abnormality caused by a partial deletion in chromosome 9. It was first described in 1973 by Alfi et al., and has since been... -
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- Clinical Implication of the Deletion Status of ABL-BCR on Derivative Chromosome 9 in Chronic Myelogenous Leukemia
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Lee YK, Kim YR, Lee DS, She CJ, Yoon SS, Park SY, Kim BK, Cho HI
- KMID: 2239626
- Korean J Lab Med.
- 2002 Dec;22(6):373-381.
BACKGROUND: The complementary ABL-BCR gene rearrangement is formed at chromosome 9 parallel to the Ph chromosome at der(22)t(9;22), which has been found deleted in a minority of chronic myelogenous leukemia... -
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- Decreased DBC1 Expression Is Associated With Poor Prognosis in Patients With Non-Muscle-Invasive Bladder Cancer
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Shim UJ, Lee IS, Kang HW, Kim J, Kim WT, Kim IY, Ryu KH, Choi YH, Moon SK, Kim YJ, Yun SJ, Lee SC, Kim WJ
- KMID: 2316122
- Korean J Urol.
- 2013 Sep;54(9):631-637.
PURPOSE: The deleted in bladder cancer 1 (DBC1) gene is located within chromosome 9 (9q32-33), a chromosomal region that frequently shows loss of heterozygosity in bladder cancer (BC). It is... -
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