Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
---|---|---|---|---|---|---|
2006 | A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease | MING CHEN ; Kuo, Shou-Jen; Liu, Chin-San; Chen, Wei-Liang; TSANG-MING KO ; Chen, Tze-Ho; Chang, Shun-Ping; Huang, Chien-Hao; Chang, Yih-Yuan; Wang, Bao-Tyan | Prenatal diagnosis | 12 | 10 | |
2004 | Prenatal Diagnosis of a Fetus Affected with down Syndrome and Deletion 1p 36 Syndrome by Fluorescence in Situ Hybridization and Spectral Karyotyping | HSIEH, TSUNG-CHE; YEH, GUANG-PERNG; CHEN, MING; WANG, BAO-TYAN | FETAL DIAGNOSIS AND THERAPY | |||
2004 | Revisit on a Distinctive Chromosome 1p36 Deletion Syndrome: Report of One Case and Review of the English Literature | LEE, MENG-LUEN; TSAO, LON-YEN; WANG, BAO-TYAN; CHIU, ING-SH | INTERNATIONAL JOURNAL OF CARDIOLOGY | |||
2003 | Trisomy 13 Manifested as Hypoplastic Left Heart and Other Structural Abnormalities | CHEN, MING; SHIH, JIN-CHUNG; WANG, BAO-TYAN | PRENATAL DIAGNOSIS |