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| 1 |
Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women
Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong
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| 2 |
Dental Treatment of Children with CATCH 22 Syndrome: Case Report
Mi Sun Kim, Soo Eon Lee, Hyo Jung Ahn, Jae-Hong Park, Sung Chul Choi
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| 3 |
The Expression of AGO2 and DGCR8 in Idiopathic Sudden Sensorineural Hearing Loss
Soon Yong Han, Shin Kim, Dong-Hoon Shin, Jae Hyun Cho, Sung-Il Nam
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| 4 |
Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome
Mi-Young Lee, Hye-Sung Won, Ju Won Baek, Jae-Hyun Cho, Jae-Yoon Shim, Pil-Ryang Lee, Ahm Kim
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| 5 |
A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman
Seung Kyung Lee, Min Jeong Lee, Hyo Jin Lee, Bu Kyung Kim, Young Bae Sohn, Yoon-Sok Chung
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| 6 |
Aspiration pneumonia in the child with DiGeorge syndrome -A case report-
Ji-Young Lee, Yun-Joung Han
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| 7 |
A Case of DiGeorge Syndrome With Ocular Manifestation
Kyoung Min Kim, Ji Woong Lee, Bo Young Chun, Jae Pil Shin, Si Yeol Kim
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| 8 |
Comparing Two Diagnostic Laboratory Tests for Several Microdeletions Causing Mental Retardation Syndromes: Multiplex Ligation-Dependent Amplification vs Fluorescent In Situ Hybridization
Eun Hae Cho, Bo Ya Na Park, Jung Hee Cho, You Sun Kang
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| 9 |
Clinical Features and Molecular Diagnosis of CATCH-22 Syndrome
Jung Yun Choi, Jeong-Wook Seo, Myoung Hee Kim, Eul Kyung Kim, Jung-Sun Kim, Ho Sung Kim, Chong Heon Lee, Hyangsuk Hur, Eun Jung Bae, Chung Il Noh, Yong Soo Yun
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