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제5차 대한간학회 춘계학술대회 초록집 : C형 간염 바이러스로 인한 만성 간질환 환자에서 HCV-RNA의 유전자형에 관한 연구
이철종 ( Lee Cheol Jong ),신우원 ( Sin U Won ),안현숙 ( An Hyeon Sug ),이성욱 ( Lee Seong Ug ),노명환 ( No Myeong Hwan ),한상영 ( Han Sang Yeong ),최석렬 ( Choe Seog Lyeol ),정진숙 ( Jeong Jin Sug ) 대한간학회 1999 Clinical and Molecular Hepatology(대한간학회지) Vol.5 No.1(S)
김문정 ( Kim Mun Jeong ),김미경 ( Kim Mi Gyeong ),박현주 ( Park Hyeon Ju ),설현주 ( Seol Hyeon Ju ),신지혜 ( Shin Ji Hye ),강문정 ( Kang Mun Jeong ),안현숙 ( An Hyeon Sug ) 대한산부인과학회 2003 Obstetrics & Gynecology Science Vol.46 No.7
The prenatal diagnosis of spina bifida includes the combined use of maternal serum α-fetoprotein (MSAFP) screening and fetal sonography. On ultrasonogram, spina bifida is characterized by visualization of the spinal defect and associated cranial abnomalities: the Lemon sign, the Banana sign, ventriculomegaly, small biparietal diameter, and obliteration of the cistema magna. We should now be able to rely on ultrasound as the main technique for diagnosis of spina bifida when MSAFP is elcvated. Recently, we have experienced three cases of spina bifida diagnosed with meningomyelocele, lemon sign, banana sign and ventriculomegaly on ultrasonogram at respectively 18^+3, 18, and 18^+6 weeks of gestation. We present these cases with a brief review of literatures.
이경순 ( Lee Gyeong Sun ),이소영 ( Lee So Yeong ),박희정 ( Park Hui Jeong ),안현숙 ( An Hyeon Sug ),박숙자 ( Park Sug Ja ),한진영 ( Han Jin Yeong ) 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.5
Tetrasomy for the short arm of chromosome 12 (Pallister-Killian syndrome) is an uncommon mosaic aneuploidy, which may present in the prenatal period with an ultrasonographically detected fetal abnormalities or following karyotyping for maternal age and other causes. In this syndrome the chromosome abnormalities, isochromosome is present in amniocyte with a much greater percentage than fetal lymphocyte. The most consistent reported prenatal ultrasound findings for tetrasomy 12p include polyhydramnios with short femurs and a diaphragmatic hernia. We report a case identified by prenatal karyotyping diagnosis.