- Cytogenetic Analysis of Squamous Cell Carcinoma of the Lung
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Jo SJ
- KMID: 2030733
- Korean J Anat.
- 1997 Oct;30(5):567-574.
The cytogenetic study of 3 cases of squamous cell carcinoma of the lung was performed to identify chromosomal abnormalities. All tumor cells were hypodiploid state on the average. Specicfic chromosomal... -
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- A Case of Azoospermia Associated with Y - Autosome Translocation
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Lee SH, Yoon TK, Cha KY, Kwak IP, Kim HJ, Nam YS
- KMID: 2261375
- Korean J Obstet Gynecol.
- 1999 Mar;42(3):625-627.
Aneuploidy results from nondisjunction in either the meiotic division of the parents or the early cleavage divisions of the affected individuals. The sex chromosomes show a wide range of viable... -
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- A Karyotype Study in Chiroptera (Bats)
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Oh YK
- KMID: 687703
- Yonsei Med J.
- 1975 Dec;16(2):47-53.
- doi: 10.3349/ymj.1975.16.2.47
The bat (Chiroptera) is the only mammal that is able to fly as birds do and forms a peculiar taxonomic group in that the diploid number of chromosomes seldom are... -
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- A Case of 21-Monosomy with Holoprosencephaly(Semilobar Type)
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Lee SY, Cho SM
- KMID: 1606978
- J Korean Pediatr Soc.
- 2003 Aug;46(8):831-835.
Holoprosencephaly of unknown definite causes, has been associated with several chromosome abnormalities involving the autosomes and the sex chromosomes. The most commonly reported associations include dup(3p), del(7q), deletions of chromosome... -
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- A Rare der(Y)t(Y;1)(q12;q12) in a Patient with Essential Thrombocythemia
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Lim HH, Choi JL, Kim BR, Woo KS, Kim KH, Kim JM, Kim SH, Han JY
- KMID: 2308735
- Lab Med Online.
- 2016 Jul;6(3):183-186.
- doi: 10.3343/lmo.2016.6.3.183
Among hematologic diseases, structural abnormalities of autosomal chromosomes are well-known, but cases involving the sex chromosomes are uncommon. Duplications of the long arm of chromosome 1 have been reported in... -
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- Periodic Explosive Expansion of Human Retroelements Associated with the Evolution of the Hominoid Primate
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Kim TM, Hong SJ, Rhyu MG
- KMID: 1733474
- J Korean Med Sci.
- 2004 Apr;19(2):177-185.
- doi: 10.3346/jkms.2004.19.2.177
Five retroelement families, L1 and L2 (long interspersed nuclear element, LINE), Alu and MIR (short interspersed nuclear element, SINE), and LTR (long terminal repeat), comprise almost half of the human... -
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- Sperm DNA fragmentation and sex chromosome aneuploidy after swim-up versus density gradient centrifugation
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Kim SW, Jee BC, Kim SK, Kim SH
- KMID: 2401622
- Clin Exp Reprod Med.
- 2017 Dec;44(4):201-206.
- doi: 10.5653/cerm.2017.44.4.201
OBJECTIVE: The aim of this study was to compare the efficacy of swim-up and density gradient centrifugation (DGC) for reducing the amount of sperm with fragmented DNA, sex chromosome aneuploidy,... -
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- A Case of 45 , X/47 , XXX Turner Syndrome Which has Experienced Pregnacy and Premature Ovarian Failure
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Nam YS, Lee SH, Kwak IP, Yoon TK, Cha KY
- KMID: 2261078
- Korean J Obstet Gynecol.
- 1998 Jul;41(7):1988-1992.
Sex chromosome monosomy occurs as monosomy X or Turner syndrome (45,X). Monosomy X is prenatally lethal in most cases, occuring in many cytogenetically abnormal spontaneous abortions. The incidence of monosomy... -
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- Pulmonary Arteriovenous Malformation in Cryptogenic Liver Cirrhosis Associated with Turner's Syndrome
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Kim JH, Jung YK, Jeong ES, Seo YS, Yim HJ, Yeon JE, Shim JJ, Byun KS, Lee CH
- KMID: 2284196
- Gut Liver.
- 2010 Jun;4(2):258-261.
Turner's syndrome is a genetic disorder of the sex chromosomes (e.g., 45,X or 45,X/46,XX) that manifests as various congenital anomalies. Despite its numerous extragonadal manifestations and frequent accompanying abnormalities in... -
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- Prenatally Diagnosed Uncommon Mosaic Autosomal Trisomy
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Lee BY, Park SY, Lee MH, Kim JW, Park JY, Choi EY, Lee YW, Oh AR, Lee SY, Kim MH, Ryu HM
- KMID: 2244898
- J Genet Med.
- 2009 Jun;6(1):95-99.
Prenatal diagnosis of rare autosome mosaicism involvingchromosomes other than chromosome 13, 18, 21 or the sex chromosome is encountered prognostic dilemma during genetic counseling. We report four cases of level... -
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- A Cytogenetic Survey of the Mentally Retarded Children
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Ju KS, Lee HK
- KMID: 2261774
- Korean J Obstet Gynecol.
- 2000 Jan;43(1):11-16.
OBJECTIVE: A cytogenetic survey of the mentally retarded children in Seoul City Welfare Center for the Mentally Retarded and St Peter school has been undertaken. METHODS: The chromosome analysis was... -
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- The Optimization of Human Sperm Decondensation Procedure for Fluorescence in Situ Hybridization
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Pang MG
- KMID: 2235771
- Korean J Fertil Steril.
- 1997 Dec;24(3):369-375.
Studies were conducted to determine the efficiency of decondensation protocols. Sperm obtained from seven normal donors was immediately washed after liquefaction and then decondensed using the method of West or... -
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- Prenatal diagnosis by isolation of fetal nucleated RBCs in maternal peripheral blood
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Jeon YJ, Kwon KH, Hwang HS, Lee SH, Pang MG, Ann JJ, Chun SH, Kim YJ
- KMID: 2077757
- Korean J Obstet Gynecol.
- 2007 Jun;50(6):850-857.
OBJECTIVE: To identify prenatal fetal sex and chromosomal aneuploidies by FISH using isolation of fetal nucleated RBCs. METHODS: peripheral blood samples was collected from 37 women between 11 and 24 weeks... -
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- A Clinical Study of Sex Chromosomal Abnormalities
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Choi OH
- KMID: 2260824
- Korean J Obstet Gynecol.
- 1997 Jun;40(6):1178-1188.
To provide current information on sex chromosome abnormalities to obstetricians andgynecologists who encounter such diagnoses and who counsel prospective parents faced withthe prenatal diagnosis of a sex chromosome abnormalities. I... -
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- Obsessive-compulsive Disorder in a Patient with 47,XXX, Triple X Syndrome
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Kim JH, Jin YH, Jang KY
- KMID: 2340377
- J Korean Neuropsychiatr Assoc.
- 1999 Sep;38(5):1186-1194.
Triple X syndrome is a relatively rare sex chromosomal anomaly, and its association with psychopathology is not well understood. The authors report one case of obsessive-compulsive disorder(OCD)with karyotype-confirmed triple X... -
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- Prenatal Diagnosis of Yq Deletion by Cytogenetic and Fluorescence in Situ Hybridization
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Park IY, Cheon SH, Kim M, Son JO, Lee Y, Shin JC, Kim CY
- KMID: 2072108
- Korean J Perinatol.
- 2004 Dec;15(4):356-361.
OBJECTIVE: The accurate evaluation of a marker chromosome has been limited during prenatal karyotyping. We proposed a method of step-by-step approach to evaluate the origin of a marker chromosome. METHODS: A... -
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- XYY syndrome: a 13-year-old boy with tall stature
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Jo WH, Jung MK, Kim KE, Chae HW, Kim DH, Kwon AR, Kim HS
- KMID: 2150395
- Ann Pediatr Endocrinol Metab.
- 2015 Sep;20(3):170-173.
- doi: 10.6065/apem.2015.20.3.170
When evaluating the underlying causes of tall stature, it is important to differentiate pathologic tall stature from familial tall stature. Various pathologic conditions leading to adult tall stature include excess... -
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- First stage reconstruction of ambiguous external genitalia in children
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Lee PK, Hong SH, Kim YJ, Lim P, Shin MS
- KMID: 2119374
- J Korean Soc Plast Reconstr Surg.
- 1998 Apr;25(3):394-400.
The criteria for the identification of sex are as follows; sex chromosome and chromatin, gonadal structure, morphology of the external genitalia, morphology of the internal genitalia, hormonal status, sex of... -
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- SRY Gene Evaluation in Patients with the Disorders of Sexual Differentiation
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Lee MC, Han SW, Lee JS, Choi SK
- KMID: 2060711
- Korean J Urol.
- 1997 Mar;38(3):299-305.
The disorders of sexual differentiation occurred due to the incompatibility of chromosomal sex, gonadal sex and phenotypic sex. A gene within Y chromosome such as SRY gene has been searched... -
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- Parental Decisions of Prenatally Detected Sex Chromosome Abnormality
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Kim YJ, Park SY, Han JY, Kim MY, Yang JH, Choi KH, Kim YM, Kim JM, Ryu HM
- KMID: 2157594
- J Korean Med Sci.
- 2002 Feb;17(1):53-57.
- doi: 10.3346/jkms.2002.17.1.53
Because of the widespread use of amniocentesis, the prenatal recognition of sex chromosome abnormality (SCA) has become increasingly common. Recent literature provided an insight into the understanding of the natural... -
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