|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"wang wayseen"
Showing items 26-75 of 201 (5 Page(s) Totally)
1 2 3 4 5 > >>
View [10|25|50] records per page
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia
|
陳持平;Chen, Chih-Ping;*;Cha, Tung-Yao;Chang, Tung-Yao;Lin, Tan-Wei;Lin, Tan-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly ;SRTD3; associated with compound heterozygous mutations in DYNC2H1 in a fetus
|
陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
|
陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2017-12 |
Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis
|
陳持平;Chen, Chih-Ping;Wa, Liang-Kai;Wang, Liang-Kai;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;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones
|
陳持平;Chen, Chih-Ping;Chen, Chen-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;Ya, Chien-Wen;Yang, Chien-Wen;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2017-10 |
Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism
|
陳持平;Chen, Chih-Ping;Tsai, Chris;Tsai, Chris;Li, Ming-Huei;Lin, Ming-Huei;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chen, Wen-Lin;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22->q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder and in
|
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;Ya, Chien-Wen;Yang, Chien-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality
|
陳持平;Chen, Chih-Ping;*;Fu, Chung-Hu;Fu, Chung-Hu;Lin, Yi-Hui;Lin, Yi-Hui;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling
|
陳持平;Chen, Chih-Ping;*;Ch, Schu-Rern;Chern, Schu-Rern;Ch, Nan-Chang;Chiu, Nan-Chang;Liu, Yu-Peng;Liu, Yu-Peng;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12->q13.1::) associated with phenotypic abnormalities
|
陳持平;Chen, Chih-Ping;*;Li, Shuan-Pei;Lin, Shuan-Pei;Lin, Yi-Hui;Lin, Yi-Hui;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
|
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;Ya, Chien-Wen;Yang, Chien-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-10 |
Mosaic trisomy 17 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
|
陳持平;Chen, Chih-Ping;*;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Wu, Peih-Shan;Wu, Peih-Shan;Town, Dai-Dyi;Town, Dai-Dyi;Pan, Chen-Wen;Pan, Chen-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-10 |
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion
|
陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Su, Yi-Ning;Su, Yi-Ning;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Che, Shin-Wen;Town, Dai-Dyi;Town, Dai-Dyi;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-10 |
Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome
|
陳持平;Chen, Chih-Ping;*;Chen, Chen-Yu;Chen, Chen-Yu;Cha, Tung-Yao;Chang, Tung-Yao;Yang, Hsiu-Yu;Yang, Hsiu-Yu;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-08 |
Prenatal diagnosis of partial monosomy 5p (5p15.1->pter) and partial trisomy 7p (7p15.2->pter) associated with cystic hygroma, abnormal skull development and ventriculomegaly
|
陳持平;Chen, Chih-Ping;*;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Ko, Kevin;Ko, Kevin;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-08 |
Rapid diagnosis of pseudomosaicism in a case of level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis
|
陳持平;Chen, Chih-Ping;*;Ch, Shing-Jyh;Chang, Shing-Jyh;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-06 |
Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay
|
陳持平;Chen, Chih-Ping;*;Chiang, Sheng;Chiang, Sheng;Kung-Liahng;Wang, Kung-Liahng;Cho, Fu-Nan;Cho, Fu-Nan;Chen, Ming;Chen, Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Shin-Wen Chen;Shun-Ping Chang;Chen, Weu-Lin;Chen, Weu-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-06 |
22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound
|
陳持平;Chen, Chih-Ping;*;Cha, Tung-Yao;Chang, Tung-Yao;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Weu-Lin;Chen, Weu-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot
|
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;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;*;Wan, Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome
|
陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
|
Chen, Yen-Ni;Chen, Yen-Ni;陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Wu, Pei-Chen;Wu, Pei-Chen;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Peih-Shan;Wu, Peih-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201502 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
|
Su, 陳持平*; Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201502 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
Wan, 陳持平*; Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Liu, Yu-Peng;Liu, Yu-Peng;Pe, Cheng-Ran;Peng, Cheng-Ran;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201502 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
|
陳持平*; Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-04 |
First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
|
陳持平*;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Yen-Ni;Chen, Yen-Ni;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
|
陳持平*;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
陳持平*;Wan, Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Liu, Yu-Peng;Liu, Yu-Peng;Pe, Cheng-Ran;Peng, Cheng-Ran;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
|
陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q; of paternal origin in a pregnancy with fetal cystic hygroma
|
陳持平;Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
|
陳持平*;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q ; of paternal origin in a pregnancy with fetal cystic hygroma
|
;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Ming-Huei;Lin, Ming-Huei;Wa, Tao-Yeuan;Wang, Tao-Yeuan;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2014-03 |
Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review
|
陳持平;Chen, Chih-Ping;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Che, Shee-Uan;Chen, Shee-Uan;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Pei-Chen;Wu, Pei-Chen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Kuo, Yu-Ling;Kuo, Yu-Ling;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes
|
陳持平;Chen, Chih-Ping;Wang, Pu-Tsui;Wang, Pu-Tsui;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Chen, Yu-Ting;Chen, Yu-Ting;Wu, Peih-Shan;Wu, Peih-Shan;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
Showing items 26-75 of 201 (5 Page(s) Totally)
1 2 3 4 5 > >>
View [10|25|50] records per page
|
