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Items for Author "Shuan-Pei Lin"
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Showing 56 items.
Collection
Date
Title
Authors
Bitstream
[生物醫學研究所] 期刊論文
2012-12-01
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yuan-Ling Huang
;
Schu-Rern Chern
;
Yu-Peng Liu
;
Jun-Wei Su
;
Chen-Chi Lee
;
Wen-Lin Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-12-01
Partial trisomy 1q (1q42.13->qter) and partial monosomy 6q (6q27->qter) in a girl with single median maxillary central incisor, dysgenesis of corpus callosum and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Jun-Wei Su
;
Chen-Chi Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-11-01
A de novo 4.4-Mb microdeletion in 2p24.3->p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Shuenn-Dyh Chang
;
Shu-Hang Ng
;
Yu-Peng Liu
;
Jun-Wei Su
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-09-01
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Jun-Wei Su
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-09-01
Partial monosomy 3p (3p26.2->pter) and partial trisomy 5q (5q34->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Yu-Peng Liu
;
Jun-Wei Su
;
Meng-Shan Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder
Chih-Ping Chen
;
Shuan-Pei Lin
;
Jun-Wei Su
;
Dai-Dyi Town
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Ming-Huei Lin
;
Jun-Wei Su
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Partial monosomy 9p (9p22.2->pter) and partial trisomy 18q (18q21.32->qter) in a female infant with anorectal malformations
Chih-Ping Chen
;
Hsien-Ming Lin
;
Cheung Leung
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Jun-Wei Su
;
Yu-Ting Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder
Chih-Ping Chen
;
Shuan-Pei Lin
;
Jun-Wei Su
;
Meng-Shan Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Jun-Wei Su
;
Schu-Rern Chern
;
Yen-Jiun Chen
;
Meng-Shan Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation
Chih-Ping Chen
;
Shuan-Pei Lin
;
Chyong-Hsin Hsu
;
Schu-Rern Chern
;
Jun-Wei Su
;
Yen-Jiun Chen
;
Chen-Wen Pan
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Pure distal 9p deletion in a female infant with cerebral palsy
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Jun-Wei Su
;
Schu-Rern Chern
;
Dai-Dyi Town
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-06-01
Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Jian-Pei Huang
;
Schu-Rern Chern
;
Jun-Wei Su
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-03-01
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Dar-Shong Lin
;
Yu-Peng Liu
;
Lee James Hsu
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2012-03-01
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Dai-Dyi Town
;
Li-Feng Chen
;
Meng-Shan Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-12-01
Pure interstitial duplication of chromosome 7q (7q31.2→q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Meng-Shan Lee
;
Yen-Jiun Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-11-01
Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis
Chia-Cheng Hung
;
Shin-Yu Lin
;
Shuan-Pei Lin
;
Chih-Ping Chen
;
Lang-Yao Chen
;
Chien-Nan Lee
;
Yi-Ning Su
[生物醫學研究所] 期刊論文
2011-09-01
A 24.2-Mb deletion of 4q12→q21.21 characterized by array CGH in a 13½-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Li-Feng Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-09-01
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-09-01
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming Chen
;
Yi-Ning Su
;
Schu-Rern Chern,
;
Tao-Yeuan Wang
;
Yu-Peng Liu
;
Fuu-Jen Tsai
;
Chen-Chi Lee
;
Yen-Jiun Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-09-01
Self-injurious behavior associated with trisomy 9p (9p13.1→p24.3)
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Wen-Lin Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-06-01
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yu-Peng Liu
;
Jeng-Daw Tsai
;
Chen-Yu Chen
;
Shin-Lin Shih,
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2011-05-01
Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene
Chia-Cheng Hung
;
Shin-Yu Lin
;
Chien-Nan Lee
;
Chih-Ping Chen
;
Shuan-Pei Lin
;
Mei-Chyn Chao
;
Shyh-Shin Chiou
;
Yi-Ning Su
[生物醫學研究所] 期刊論文
2011-03-01
Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Fuu-Jen Tsai
;
Schu-Rern Chern
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Meng-Shan Lee
;
Yu-Ting Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-12-01
A 5.3-Mb duplication of 9p12→p13.1 characterized by array CGH in a female infant with developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Fuu-Jen Tsai,
;
Chen-Chi Lee
;
Chen-Wen Pan
;
Pei-Chen Wu
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-12-01
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin
;
Ming-Ren Chen
;
Ching-Chi Lin
;
Chih-Ping Chen
;
Dar-Shong Lin
;
Chih-Kuang Chuang
;
Dau-Ming Niu
;
Jui-Hung Chang
;
Hung-Chang Lee
;
Shuan-Pei Lin
[生物醫學研究所] 期刊論文
2010-09-01
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
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Yu-Ting Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-09-01
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and dsomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
Chih-Ping Chen
;
Yung-Ting Guo
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Yann-Jang Chen
;
Rui-Yuan Hseuh
;
Yi-Hui Lin
;
Pei-Chen Wu
;
Chen-Chi Lee,
;
Yu-Ting Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-09-01
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses
Chih-Ping Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Yu-Ming Hwu
;
Shuan-Pei Lin
;
Chyong-Hsin Hsu
;
Fuu-Jen Tsai
;
Tao-Yeuan Wang
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Yu-Ting Chen
;
Li-Feng Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-07-01
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2→q24.3 in a girl with autistic features and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Yann-Jang Chen
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-06-01
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux including polyhydramnios in the third trimester
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Chen-Yu Chen
;
Fuu-Jen Tsai
;
Yu-Peng Liu
;
Schu-Rern Chern
;
Pei-Chen Wu
;
Hsaio-En Cindy Chen
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2010-06-01
Deletion 2q37.3→qter and duplication 15q24.3→qter characterized by array CGH in a girl with epilepsy and dysmorphic features
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Li-Feng Chen
;
Meng-Shan Lee
;
Wayseen Wang.
[生物醫學研究所] 期刊論文
2010-02-01
Prenatal diagnosis of X-linked myotubular myopathy
Chih-Ping Chen
;
Shuan-Pei Lin
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Tao-Yeuan Wang
;
Hung-Hung Lin
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2009-11-01
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
Chia-Cheng Hung
;
Shin-Yu Lin
;
Chien-Nan Lee
;
Hui-Yu Cheng
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Chih-Ping Chen
;
Chien-Hui Chang
;
Chiou-Ya Lin
;
Chih-Chieh Yu
;
Hsin-Hui Chiu,
;
Wen-Fang Cheng
;
Hong-Nerng Ho
;
Dau-Ming Niu
;
Yi-Ning Su
[生物醫學研究所] 期刊論文
2008-10-01
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review
Chih-Ping Chen
;
Shuan-Pei Lin
;
Fuu-Jen Tsai
;
Tzu-Hao Wang
;
Schu-Rern Chern
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2008-08-01
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients
Wei-De Lin
;
Shuan-Pei Lin
;
Chung-Hsing Wang
;
Wuh-Liang Hwu
;
Chih-Kuang Chuang
;
Shio-Jean Lin
;
Yushin Tsai
;
Chih-Ping Chen
;
Fuu-Jen Tsai.
[生物醫學研究所] 期刊論文
2008-07-01
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Fuu-Jen Tsai
;
Schu-Rern Chern
;
Chen-Chi Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2008-06-01
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Shu-Chin Chien
;
Fuu-Jen Tsai
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2008-06-01
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
Chih-Ping Chen
;
Shuan-Pei Lin
;
Fuu-Jen Tsai
;
Schu-Rern Chern
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2008-06-01
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings
Chih-Ping Chen
;
Shuan-Pei Lin
;
Fuu-Jen Tsai
;
Hung-Hung Lin
;
Schu-Rern Chern
;
Chih-Kuang Chuang
;
Chen-Chi Lee
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2008-01-01
The -590 C/T and 8375 A/G interleukin-4 polymorphisms are not associated with Kawasaki disease in Taiwanese children.
Fu-Yuan Huang
;
Tzu-Yang Chang
;
Ming-Ren Chen
;
Hung-Chang Lee
;
Nan-Chang Chiu
;
Hsin Chi
;
Chyong-Hsin Hsu
;
Shuan-Pei Lin
;
Hsin-Fu Liu
;
Wei-Fang Chen
;
Chen-Chung Chu
;
Marie Lin
;
Yann-Jinn Lee
[生物醫學研究所] 期刊論文
2007-12-01
Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly
Chih-Ping Chen
;
Shuan-Pei Lin
;
Tung-Yao Chang
;
Hsin-Tsung Ho
[生物醫學研究所] 期刊論文
2007-09-01
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1
Wei-De Lin
;
Shuan-Pei Lin
;
Chih-Ping Chen
;
Fuu-Jen Tsai
[生物醫學研究所] 期刊論文
2007-09-01
Perinatal imaging findings of Galloway-Mowat syndrome
Chih-Ping Chen.
;
Shuan-Pei Lin
;
Jeng-Daw Tsai
;
Jon-Kway Huang
;
Jui-Lung Yen
;
Ching-Chang Tseng
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2007-09-01
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Tung-Yao Chang
;
Hung-Chang Lee
;
Han-Yang Hung
;
Hsiang-Yu Lin
;
Jian-Pei Huang
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2007-06-01
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin
;
Shuan-Pei Lin
;
Chih-Kuang Chuang
;
Ming-Ren Chen
;
Jui-Lung Yen
;
Yann-Jinn Lee
;
Chi-Yu Huang
;
Li-Ping Tsai
;
Dau-Ming Niu
;
Mei-Chyn Chao
;
Pao-Lin Kuo
[生物醫學研究所] 期刊論文
2007-03-01
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)
Chih-Ping Chen
;
Shuan-Pei Lin
;
Chin-Yuan Tzen
;
Wuh-Liang Hwu
;
Schu-Rern Chern
;
Chih-Kuang Chuang
;
Shu-Shien Chiang
;
Wayseen Wang
[生物醫學研究所] 期刊論文
2007-03-01
Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin
;
Shuan-Pei Lin
;
Jui-Lung Yen
;
Yann-Jinn Lee
;
Chi-Yu Huang
;
Han-Yang Hung
;
Chyong-Hsin Hsu
;
Hsin-An Kao
;
Jui-Hsing Chang
;
Nan-Chang Chiu
;
Che-Sheng Ho
;
Mei-Chyn Chao
;
Dan-Ming Niu
;
Li-Ping Tsai
;
Pao-Lin Kuo
[生物醫學研究所] 期刊論文
2003-06-01
Percutaneous endoscopic gastrostomy in children: 15 cases experience
Ting-Chi Yeh
;
Chun Yan Yeung
;
Jin-Cherng Sheu
;
Hung-Chang Lee
;
Shuan-Pei Lin
;
Chyong-Hsin Hsu
;
Yann-Jinn Lee
;
Nan-Chang Chiu
;
Che-Sheng Ho
[生物醫學研究所] 期刊論文
2002-01-01
Airway changes in children with mucopolysaccharidoses: CT evaluation
Shin-Lin Shih
;
Yann-Jinn Lee
;
Shuan-Pei Lin
;
Chin-Yin Sheu
;
Johan G. Blickman
[生物醫學研究所] 期刊論文
1999-02-01
Congenital nasal pyriform aperture stenosis: A diagnostic clue to solitary maxillary central incisor prior to eruption in three infants
Fu-Sung Lo
;
Kuo-Sheng Lee
;
Lih-Sheng Chen
;
Han-Yang Hung
;
Chyong-Hsin Hsu
;
Shuan-Pei Lin
;
Yann-Jinn Lee
[聽力暨語言治療學系] 期刊論文
2014-04-01
Assessment of hearing loss by pure-tone audiometry in patients with mucopolysaccharidoses
Hsiang-Yu Lin
;
Shou-Chuan Shih
;
Chih-Kuang Chuang
;
Kuo-Sheng Lee
;
Ming-Ren Chen
;
Hung-Ching Lin
;
Pao Chin Chiu
;
Dau-Ming Niu
;
Shuan-Pei Lin
[聽力暨語言治療學系] 期刊論文
2011-06-01
Other impairment associated with developmental language delay in preschool-aged children
Yao-Chia Chuang
;
Chia-Yu Hsu
;
Nan-Chang Chiu
;
Shuan-Pei Lin
;
Ruu-Fen Tzang
;
Cheng-Chien Yang
[醫學系] 期刊論文
2011-05-01
Sebaceous nevus syndrome, central nervous system malformations, aplasia cutis congenita, limbal dermoid, and pigmented nevus syndrome
Chih-Wei Hsieh
;
Yu-Hung Wu
;
Shuan-Pei Lin
;
Chun-Chih Peng
;
Che-Sheng Ho
[醫學系] 期刊論文
2009-12-01
Lafora disease and congenital generalized lipodystrophy: a case report
Chih-Fan Tseng
;
Che-Sheng Ho
;
Nan-Chang Chiu
;
Shuan-Pei Lin
;
Chi-Yuan Tzen
;
Yu-Hung Wu
[醫學系] 期刊論文
2002-01-01
Bilateral calcified ovarian fibromas in a patient with Sotos syndrome
Chih-Ping Chen
;
Yuh-Cheng Yang
;
Shuan-Pei Lin
;
Wayseen Wang
;
Chih-Long Chang
;
Kuo-Ming Chang
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