|
|
???tair.name??? >
???browser.page.title.author???
|
"wang wayseen"???jsp.browse.items-by-author.description???
Showing items 86-135 of 201 (5 Page(s) Totally)
<< < 1 2 3 4 5 > >>
View [10|25|50] records per page
| 亞洲大學 |
201309 |
Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
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 |
| 亞洲大學 |
201309 |
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 |
| 亞洲大學 |
201309 |
Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of
|
陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Guo, Wan-Yuo;Guo, Wan-Yuo;Su, Yi-Ning;Su, Yi-Ning;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II
|
陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Li, Ming-Huei;Lin, Ming-Huei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review
|
陳持平;Chen, Chih-Ping;Wang, Kuo-Gon;Wang, Kuo-Gon;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis
|
陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth
|
陳持平;Chen, Chih-Ping;Ch, Shing-Jyh;Chang, Shing-Jyh;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
|
陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome
|
陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Su, Jun-Wei;Wang, Wayseen; |
| 亞洲大學 |
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 |
| 亞洲大學 |
2013-07 |
Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;Hu, Ming-Chao;Huang, Ming-Chao;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review
|
陳持平;Chen, Chih-Ping;Cheng, Po-Jen;Cheng, Po-Jen;Shuenn-Dyh, C;Chang, Shuenn-Dyh;Lee, Yi-Xuan;Lee, Yi-Xuan;Sh, Jin-Chung;Shih, Jin-Chung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene
|
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;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
|
陳持平;Chen, Chih-Ping;Cha, Yao-Lung;Chang, Yao-Lung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20
|
陳持平;Chen, Chih-Ping;Shuenn-Dyh, C;Chang, Shuenn-Dyh;Chueh, Ho-Yen;Chueh, Ho-Yen;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction
|
陳持平;Chen, Chih-Ping;Hs, Chin-Yuan;Hsu, Chin-Yuan;Su, Yi-Ning;Su, Yi-Ning;Wa, Tao-Yeuan;Wang, Tao-Yeuan;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
|
陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism
|
陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-01 |
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome
|
陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Ma, Gwo-Chin;Ma, Gwo-Chin;Su, Yi-Ning;Su, Yi-Ning;Tsang-Ming, K;Ko, Tsang-Ming;Lin, Yi-Hui;Lin, Yi-Hui;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
|
陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Alan Hwa-Ruey Hsieh, ;Hsieh, Alex Hwa-Jiun;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis
|
陳持平;Chen, Chih-Ping;Chen-Wen Pan, ;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes
|
陳持平;Chen, Chih-Ping;Dai-Dyi Town, ;Wen-Lin Chen, ;Chen, Li-Feng;Meng-Shan Lee, ;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2012-06 |
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
|
陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Chen-Chi Lee, ;Town, Dai-Dyi;Wang, Wayseen |
| 亞洲大學 |
2012-03 |
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism
|
陳持平;Chen, Chih-Ping;Yu-Ting Chen, ;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2011-12 |
A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
|
陳持平;Chen, Chih-Ping;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
|
陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses
|
陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wang, Wayseen |
| 亞洲大學 |
2011-06 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis
|
陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wen-Lin Chen, ;Wang, Wayseen |
| 亞洲大學 |
2011-03 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations
|
陳持平;Chen, Chih-Ping;Yi-Yung Chen, ;Wang, Wayseen |
| 國立臺灣大學 |
2011 |
Mosaic Supernumerary R(1)(P13.2q23.3) in a 10-Year-Old Girl with Epilepsy, Facial Asymmetry, Psychomotor Retardation, Kyphoscoliosis, Dermatofibrosarcoma and Multiple Exostoses
|
陳持平; 林炫沛; 陳明; 蘇怡寧; 陳樹人; 王道遠; 劉育朋; 蔡輔仁; 李貞?; 陳燕彰; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; CHEN, MING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; LIU, YU-PENG; TSAI, FUU-JEN; LEE, CHEN-CHI; CHEN, YANN-JANG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis and Molecular Cytogenetic Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Ring Chromosome 4
|
陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 吳佩臻; 陳麗鳳; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review
|
陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
2010-12 |
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea
|
陳持平;Chen, Chih-Ping;Chiang, Ming-Chou;Wang, Tzu-Hao;Hsueh, Chuen;Chang, Shueen-Dyh;Tsai, Fuu-Jen;Wang, Chao-Ning;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
2010-12 |
Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Young, Richard Shih-Hung;Tsai, Fuu-Jen;Wu, Pei-Chen;Chern, Schu-Rern;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
| 亞洲大學 |
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 |
Showing items 86-135 of 201 (5 Page(s) Totally)
<< < 1 2 3 4 5 > >>
View [10|25|50] records per page
|
