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Showing items 61-85 of 99  (4 Page(s) Totally)
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Institution Date Title Author
國家衛生研究院 2010-02 Growth and thyroid function in children with in utero exposure to dioxin: A 5-year follow-up study Su, PH;Chen, JY;Chen, JW;Wang, SL
中山醫學大學 2009 Benign familial neonatal convulsions: novel mutation in a newborn. Lee, IC; Chen, JY; Chen, YJ; Yu, JS; Su, PH
中山醫學大學 2009 Posthemorrhagic hydrocephalus in newborns: clinical characteristics and role of ventriculoperitoneal shunts. Lee, IC; Lee, HS; Su, PH; Liao, WJ; Hu, JM; Chen, JY
國家衛生研究院 2008-08 Transthyretin levels are not related to Apgar score in low birth weight and very low birth weight infants Su, PH;Wang, SL;Chen, JY;Hu, JM;Chang, HP;Chen, SJ
國家衛生研究院 2008-03 A study of anthropomorphic and biochemical characteristics in girls with central precocious puberty and thelarche variant Su, PH; Wang, SL; Chen, JY; Chen, SJ; Ke, JC
中山醫學大學 2008 Sacral dysgenesis associated with terminal deletion of chromosome 7 (q36-qter). Su, PH; Chen, JY; Chen, SJ; Tsao, TF; Lai, YJ
中山醫學大學 2008 Terminal deletion of chromosome 6q. Su, PH; Chen, JY; Chen, SJ; Yang, KC
中山醫學大學 2008 Trisomy 18 syndrome with incomplete Cantrell syndrome. Hou, YJ; Chen, FL; Ng, YY; Hu, JM; Chen, SJ; Chen, JY; Su, PH
中山醫學大學 2008 Hydranencephaly associated with interruption of bilateral internal carotid arteries. Quek, YW; Su, PH; Tsao, TF; Chen, JY; Ng, YY; Hu, JM; Chen, SJ
中山醫學大學 2008 A study of anthropomorphic and biochemical characteristics in girls with central precocious puberty and thelarche variant. Su, PH; Wang, SL; Chen, JY; Chen, SJ; Ke, JC
中山醫學大學 2008 Transthyretin levels are not related to Apgar score in low birth weight and very low birth weight infants. Su, PH; Wang, SL; Chen, JY; Hu, JM; Chang, HP; Chen, SJ
中山醫學大學 2008 Anterior mediastinal immature teratoma with precocious puberty in a child with Klinefelter syndrome. Su, PH; Luh, SP; Yieh, DM; Chen, JY; Chen, SJ; Hung, HM; Liao, PF
國家衛生研究院 2007-06 Estimating final height from parental heights and sex in Taiwanese Su, PH; Wang, SL; Chen, JY
中山醫學大學 2007 Mutations and new polymorphic changes in the TCOF1 gene of patients with oculo-auriculo-vertebral spectrum and Treacher-Collins syndrome. Su, PH; Yu, JS; Chen, JY; Chen, SJ; Li, SY; Chen, HN
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
國家衛生研究院 2005-11 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

Showing items 61-85 of 99  (4 Page(s) Totally)
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