- Identification of a Fibrillin-1 Gene Mutation in a Monozygotic Twin Presenting with Bilateral Juvenile-onset Ectopia Lentis
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Yum HR, Kim SE, Shin SY, Park SH
- KMID: 2360145
- Korean J Ophthalmol.
- 2015 Feb;29(1):77-78.
- doi: 10.3341/kjo.2015.29.1.77
No abstract available. -
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- Blood Chimerism in a Dizygotic Dichorionic Pregnancy
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Jang JH, Jung H, Kim JH, Park WS, Kim SH
- KMID: 1022045
- Korean J Lab Med.
- 2010 Oct;30(5):521-524.
- doi: 10.3343/kjlm.2010.30.5.521
Blood chimerism in twins is known to occur through the transfer of hematopoietic stem cells between the fetuses via a common placenta. We present a case of blood chimerism in... -
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- Identification of a Novel Deletion Region in 3q29 Microdeletion Syndrome by Oligonucleotide Array Comparative Genomic Hybridization
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Seo EJ, Jun KR, Yoo HW, Yoo HK, Lee JO
- KMID: 1096822
- Korean J Lab Med.
- 2010 Feb;30(1):70-75.
- doi: 10.3343/kjlm.2010.30.1.70
BACKGROUND: The 3q29 microdeletion syndrome is a genomic disorder characterized by mental retardation, developmental delay, microcephaly, and slight facial dysmorphism. In most cases, the microdeletion spans a 1.6-Mb region between... -
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