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Showing items 76-85 of 100  (10 Page(s) Totally)
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Institution Date Title Author
中山醫學大學 2007 Trisomy 18 with multiple rare malformations: report of one case. Su, PH; Chen, JY; Hsu, CH; Chen, SJ; Chan, SW; Lin, LL
中山醫學大學 2007 Deletion of chromosome region 18q21.3-->qter in a patient: clinical, endocrine and imaging abnormalities. Su, PH; Chen, JY; Chen, SJ; Yang, MS; Kao, IW; Tsai, CY
中山醫學大學 2007 Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression. Su, PH; Kuo, PL; Chen, SJ; Chen, JY; Yu, JS; Liu, YL; Kao, IW
國立臺灣大學 2006-05 In utero exposure to dioxins and polychlorinated biphenyls and its relations to thyroid function and growth hormone in newborns. Wang, SL; Su, PH; Jong, SB; Guo, YL; Chou, WL; Papke, O.
中山醫學大學 2006 Short stature in patients with 45,X/46,XY mosaicism: report of three cases. Lee, CF; Su, PH; Chen, JY; Chen, SJ; Yang, KC; Lin, LL
中山醫學大學 2006 Neonatal startle disease with severe apnea episodes: report of one case. Lee, IC; Sheu, JN; Su, PH; Chen, JY
中山醫學大學 2006 45,X/46,XX mosaicism in a mother and one of her discordant monozygotic twin daughters: report of one case. Su, PH; Chen, JY; Chen, SJ; Hung, HM; Ting, HC; Lin, CY; Quek, YW
中山醫學大學 2006 Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q. Su, PH; Chen, JY; Chen, SJ; Yang, MS; Liu, YL
中山醫學大學 2006 Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case. Ng, YY; Hu, JM; Su, PH; Chen, JY; Yang, MS; Chen, SJ
中山醫學大學 2006 Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene. Su, PH; Chen, JY; Chen, SJ; Yu, JS

Showing items 76-85 of 100  (10 Page(s) Totally)
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