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    Items for Author "Lee, Chen-Chi" 

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    Showing 43 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 2018-02 Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities 陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2018-02 Late-onset fetal bilateral pleural effusions associated with Down syndrome La, Shih-Ting; 陳持平; Chen, Chih-Ping; *; Lin, Chen-Ju; Lin, Chen-Ju; Hs, Chin-Yuan; Hsu, Chin-Yuan; Wu, Peih-Shan; Wu, Peih-Shan; Lee, Chen-Chi; Lee, Chen-Chi; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2017-12 Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome 陳持平; Chen, Chih-Ping; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2017-12 Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound 陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2017-12 Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1 陳持平; Chen, Chih-Ping; Hs, Chih-Heng; Hsieh, Chih-Heng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-12 Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome 陳持平; Chen, Chih-Ping; *; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-10 Molecular cytogenetic characterization of Xp22.32->pter deletion and Xq26.3->qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3), a hypoplastic left heart, short stature and maternal X chromosome pericentric inversion 陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-10 Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome 陳持平; Chen, Chih-Ping; *; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Town, Dai-Dyi; Town, Dai-Dyi; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-08 Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication 陳持平; Chen, Chih-Ping; *; Lin, Chen-Ju; Lin, Chen-Ju; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-06 Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction 陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Huan, Wen-Chu; Huang, Wen-Chu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen-Wen Pan; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-06 Molecular cytogenetic characterization of inv dup del;8p; in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction 陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Huan, Wen-Chu; Huang, Wen-Chu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen-Wen Pan; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter) 陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p ;3p26.3->pter; and partial trisomy 16q ;16q23.1->qter; 陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2014-03 A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation 陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2014-03 Chromosomal deletions detected at amniocentesis Lin, Chen-Ju; Lin, Chen-Ju; 陳持平; Chen, Chih-Ping; Chi, Shu-Chin; Chien, Shu-Chin; Lee, Chen-Chi; Chen-Chi Lee,; Town, Dai-Dyi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Wen-Lin; Che, L i-Feng; Chen, L i-Feng; Le, Meng-Shan; Lee, Meng-Shan; Chen-Wen Pan,; Ku-Chien Lin,; Yeh, Tze-Tien; Yeh, Tze-Tien
    [生物科技學系] 期刊論文 An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy 陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism 陳持平; Chen, Chih-Ping; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Li-Feng Chen,; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1->pter) and 14q (14q32.31->qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction and single umbilical artery: prenatal diagnosis and molecular 陳持平; Chen, Chih-Ping; Fu, Chung-Hu; Fu, Chung-Hu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2013-10 An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy 陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2013-07 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing 陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2013-04 Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization 陳持平; Chen, Chih-Ping; Lin, Chen-Ju; Lin, Chen-Ju; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay 陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Pan, Chen-Wen; Wu, Pei-Chen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Balanced reciprocal translocations at amniocentesis 陳持平; Chen, Chih-Ping; Wu, Pei-Chen; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平; Chen, Chih-Ping; Chen, Ming; Su, Yi-Ning; Hsu, Chin-Yuan; Tsai, Fuu-Jen; Chern, Schu-Rern; Wu, Pei-Chen; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平; Chen, Chih-Ping; Su, Yi-Ning; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Chern, Schu-Rern; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Wen-Lin; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平; Chen, Chih-Ping; Chen, Ming; Ko, Tsang-Ming; Ma, Gwo-Chin; Tsai, Fuu-Jen; Tsai, Ming-Song; Wu, Pei-Chen; Lee, Chen-Chi; Che, Li-Feng; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Lin, Hung-Hung; Wu, Pei-Chen; Lee, Chen-Chi; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-12 Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling 陳持平; Chen, Chih-Ping; Huang, Ming-Chao; Su, Yi-Ning; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Town, Dai-Dyi; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings 陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平; Chen, Chih-Ping; Guo, Yung-Ting; Lin, Shuan-Pei; Su, Yi-Ning; Chen, Yann-Jang; Hseuh, Rui-Yuan; Lin, Yi-Hui; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chern, Schu-Rern; Hwu, Yu-Ming; Lin, Shuan-Pei; Hsu, Chyong-Hsin; Tsai, Fuu-Jen; Wang, Tao-Yeuan; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Chen, Li-Feng; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平; Chen, Chih-Ping; Lin, Hsien-Ming; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Ko, Tsang-Ming; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Yu-Ting; Wu, Pei-Chen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Wen-Ling; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-09 Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q 陳持平; Chen, Chih-Ping; Tsai, Fuu-Jen; Lee, Chen-Chi; Chen, Wen-Lin; Pan, Chen-Wen; Wu, Pei-Chen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-06 Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features 陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Li-Feng; Lee, Meng-Shan; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-06 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chen, Yu-Ting; Chern, Schu-Rern; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-03 Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization 陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2010-03 Unbalanced and balanced heterologous Robertsonian translocations involving chromosome 21 at amniocentesis 陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wu, Pei-Chen; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2009-12 Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis 陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chiang, Shu-Shien; Wang, Wayseen
    [生物科技學系] 期刊論文 2009-12 Trisomy 13 mosaicism associated with cyclopia and cystic hygroma 陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Wang, Wayseen
    [生物科技學系] 期刊論文 2009-12 Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis 陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wu, Pei-Chen; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen
    [生物科技學系] 期刊論文 2009-01 A 12 Mb deletion of 6p24.1 -> pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys 陳持平; Chen, Chih-Ping; Tzen, Chin-Yuan; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Lee, Chen-Chi; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen

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