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1

Application of FTA® sample collection and DNA purification system on the determination of CTG trinucleotide repeat size by PCR-based southern blotting

Kuang-Ming Hsiao, Her-Maw Lin, Huichin Pan, Tung-Cheng Li, Sung-Sheng Chen, Shuo-Bin Jou, Ya-Lan Chiu, Ming-Fang Wu, Chyi-Chyang Lin, Shuan-You Li

Journal:

Journal of Clinical Laboratory Analysis

Year:

1999

Language:

english

File:

PDF, 77 KB

english, 1999

2

Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Hui-Min Hua, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 183 KB

english, 2006

3

Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter)

Chih-Ping Chen, Chyi-Chyang Lin, Tung-Yao Chang, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 184 KB

english, 2006

4

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion

Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Tzu-Hao Wang, Chen-Chi Lee, Chen-Wen Pan, Lie-Jiau Hsieh, Wayseen Wang

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 145 KB

english, 2005

5

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yann-Jang Chen, Schu-Rern Chern, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 162 KB

english, 2006

6

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

Pi-Lin Sung, Sheng-Ping Chang, Kuo-Chang Wen, Chia-Ming Chang, Ming-Jie Yang, Lin-Chao Chen, Kuan-Chong Chao, Chi-Ying F. Huang, Yueh-Chun Li, Chyi-Chyang Lin

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 241 KB

english, 2009

7

Rare rearrangements: A “jumping satellite” in one family and autosomal location of the SRY gene in an XX male

Shu-Chin Chien, Yueh-Chun Li, Ming Ho, Pei-Ching Hsu, Ru-Hsiou Teng, Wei-De Lin, Fuu-Jen Tsai, Chyi-Chyang Lin

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 205 KB

english, 2009

8

A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1–9q33.1 deletion in a girl with a cleft lip and palate

Shu-Chin Chien, Yueh-Chun Li, Ling-Hui Li, Jer-Yuarn Wu, Pei-Ching Hsu, Sue-Lin Shi, Fuu-Jen Tsai, Chyi-Chyang Lin

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 178 KB

english, 2010

9

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter)

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Schu-Rern Chern, Wei-Min Chen, Chen-Chi Lee, Lie-Jiau Hsieh, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 266 KB

english, 2005

10

Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2→qter) and partial monosomy 5p (5p15.3→pter)

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 159 KB

english, 2005

11

Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 → pter) and partial monosomy 9p (9p22 → pter)

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Schu-Rern Chern, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 157 KB

english, 2005

12

Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Chyi-Chyang Lin, Yueh-Chun Li, Chen-Chi Lee, Lie-Jiau Hsieh, Wen-Lin Chen, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 139 KB

english, 2006

13

Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Wen-Lin Chen, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 280 KB

english, 2006

14

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)

Chih-Ping Chen, Schu-Rern Chern, Chyi-Chyang Lin, Tzu-Hao Wang, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Hui-Min Hua, Wayseen Wang

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 277 KB

english, 2006

15

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype

Chyi-Chyang Lin, Yao-Yuan Hsieh, Chung-Hsing Wang, Yueh-Chun Li, Lie-Jiau Hsieh, Chien-Chung Lee, Chang-Hai Tsai, Fuu-Jen Tsai

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 758 KB

english, 2006

16

Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding

Ni-Chung Lee, Shun-Ping Chang, Cheng-Shyong Chang, Chia-Hsiang Chen, Dong-Jay Lee, Chyi-Chyang Lin, Wuh-Liang Hwu, Ming Chen

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 125 KB

english, 2009

17

Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature

Chih-Ping Chen, Chyi-Chyang Lin, Yueh-Chun Li, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Men-Shan Lee, Wayseen Wang, Chin-Yuan Tzen

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 239 KB

english, 2004

18

The predominance of heterozygotes found in wild goldfish of lake Erie at the gene locus for sorbitol dehydrogenase

Chyi-Chyang Lin, Gisela Schipmann, William A. Kittrell, Susumu Ohno

Journal:

Biochemical Genetics

Year:

1969

Language:

english

File:

PDF, 288 KB

english, 1969

19

Higher-Order Organization of Subrepeats and the Evolution of Cervid Satellite I DNA

Charles Lee, Dean R. Court, Charles Cho, Jennifer L. Haslett, Chyi-Chyang Lin

Journal:

Journal of Molecular Evolution

Year:

1997

Language:

english

File:

PDF, 620 KB

english, 1997

20

Complex genomic organization of Indian muntjac centromeric DNA

Ya-Ming Cheng, Tzai-Shiuan Li, Lie-Jiau Hsieh, Pei-Ching Hsu, Yueh-Chun Li, Chyi-Chyang Lin

Journal:

Chromosome Research

Year:

2009

Language:

english

File:

PDF, 475 KB

english, 2009

21

Intragenic microdeletion ofRUNX2is a novel mechanism for cleidocranial dysplasia

Ming Ta Michael Lee, Anne Chun-Hui Tsai, Ching-Heng Chou, Feng-Mei Sun, Li-Chen Huang, Pauline Yen, Chyi-Chyang Lin, Chih-Yang Liu, Jer-Yuarn Wu, Yuan-Tsong Chen, Fuu-Jen Tsai

Journal:

The HUGO Journal

Year:

2008

Language:

english

File:

PDF, 252 KB

english, 2008

22

Cervid satellite DNA and karyotypic evolution of Indian muntjac

Yueh-Chun Li, Chyi-Chyang Lin

Journal:

Genes & Genomics

Year:

2012

Language:

english

File:

PDF, 309 KB

english, 2012

23

Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1

Pan, Huichin, Lin, Her-Mau, Ku, Wei-Yao, Li, Tung-Cheng, Li, Shuan-Yow, Lin, Chyi-Chyang, Hsiao, Kuang-Ming

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 92 KB

english, 2001

24

Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan

Wang, Yi-Chun, Kung, Chiu-Yun, Su, Mao-Chang, Su, Ching-Chyuan, Hsu, Hsiu-Mei, Tsai, Chin-Chu, Lin, Chyi-Chyang, Li, Shuan-Yow

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 69 KB

english, 2002

25

Interstitial colocalization of two cervid satellite DNAs involved in the genesis of the Indian muntjac karyotype

Yueh-Chun Li, Charles Lee, Despina Sanoudou, Tzong-Hsiung Hsu, Shuan-Yow Li, Chyi-Chyang Lin

Journal:

Chromosome Research

Year:

2000

Language:

english

File:

PDF, 769 KB

english, 2000

26

Conservation of Human Gamma-X Centromeric Satellite DNA Among Primates with an Autosomal Localization in Certain Old World monkeys

Charles Lee, Roscoe Stanyon, Chyi-chyang Lin, Malcolm A. Ferguson-smith

Journal:

Chromosome Research

Year:

1999

Language:

english

File:

PDF, 91 KB

english, 1999

27

Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation

Chih-Ping Chen, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Wayseen Wang

Journal:

Fertility and Sterility

Year:

2006

Language:

english

File:

PDF, 82 KB

english, 2006

28

Use of a cytogenetic whole-genome comparison to resolve phylogenetic relationships among three species: Implications for mammalian systematics and conservation biology

Hon-Tsen Yu, Gwo-Chin Ma, Dong-Jay Lee, Shih-Chien Chin, Ting-Li Chen, Hsien-Shao Tsao, Wen-Hsiang Lin, Sheng-Hai Wu, Chyi-Chyang Lin, Ming Chen

Journal:

Year:

2012

Language:

english

File:

PDF, 2.60 MB

english, 2012

29

Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial Monosomy 11q (11q23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System

Chih-Ping Chen, Tzu-Hao Wang, Chyi-Chyang Lin, Fuu-Jen Tsai, Lie-Jiau Hsieh, Wayseen Wang

Journal:

Journal of the Formosan Medical Association

Year:

2008

Language:

english

File:

PDF, 583 KB

english, 2008

30

Partial Trisomy 3p and Monosomy 7p Associated with Tetralogy of Fallot and Infantile Seizure

Chia-Ming Chang, Ming-Jie Yang, Chyi-Chyang Lin, Yueh-Chun Li, Pi-Lin Sung, Pi-Chang Lee, Lin-Chao Chen, Lie-Jiau Hsieh, Kwei-Shuai Hwang, Chih-Ping Chen, Kuan-Chong Chao

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2007

Language:

english

File:

PDF, 603 KB

english, 2007

31

Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal Male External Genitalia and a Literature Review

Shu-Chin Chien, Chih-Ping Chen, Chyi-Chyang Lin, Li-Chia Huang, Cheng-Tiao Hsieh, Fuu-Jen Tsai

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2009

Language:

english

File:

PDF, 164 KB

english, 2009

32

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

Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Ju-Ting Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2010

Language:

english

File:

PDF, 452 KB

english, 2010

33

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21

Chih-Ping Chen, Chyi-Chyang Lin, Tsang-Ming Ko, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Pei-Chen Wu, Wayseen Wang

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2010

Language:

english

File:

PDF, 218 KB

english, 2010

34

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22

Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Wen-Ling Chen, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2010

Language:

english

File:

PDF, 267 KB

english, 2010

35

Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly

Pi-Lin Sung, Chia-Ming Chang, Chih-Yao Chen, Peng-Hui Wang, Kuan-Chong Chao, Kuo-Chang Wen, Yung-Yung Cheng, Yueh-Chun Li, Chyi-Chyang Lin

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2012

Language:

english

File:

PDF, 1.04 MB

english, 2012

36

Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract

Chang, Yu-Tzu, Chou, I-Ching, Wang, Chung-Hsing, Chin, Zheng-Nan, Kuo, Huang-Tsung, Lin, Chyi-Chyang, Tsai, Chang-Hai, Tsai, Fuu-Jen

Journal:

Pediatrics & Neonatology

Year:

2013

Language:

english

File:

PDF, 530 KB

english, 2013

37

Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats

Li, Yueh-Chun, Chien, Shu-Chin, Setlur, Sunita R., Lin, Wei-De, Tsai, Fuu-Jen, Lin, Chyi-Chyang

Journal:

Journal of the Formosan Medical Association

Year:

2015

Language:

english

File:

PDF, 915 KB

english, 2015

38

SPONTANEOUS MEIOTIC CHROMOSOME ABNORMALITIES IN MALE MICE ( MUS MUSCULUS )

Lin, Chyi-Chyang, Tsuchida, W. S., Morris, S. A.

Journal:

Canadian Journal of Genetics and Cytology

Year:

1971

Language:

english

File:

PDF, 638 KB

english, 1971

39

Organization and evolution of a novel cervid satellite DNA with yeast CDEI-like repeats

Hsieh, Lei-Jiau, Cheng, Ya-Ming, Wang, Yi-Chun, Lin, Chyi-Chyang, Li, Yueh-Chun

Journal:

Zoological Studies

Year:

2014

Language:

english

File:

PDF, 2.55 MB

english, 2014

40

Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication

Li, Yueh-Chun, Pan, Yi-Ju, Tsai, Fuu-Jen, Lin, Chyi-Chyang

Journal:

Genes & Genomics

Year:

2016

Language:

english

File:

PDF, 1.46 MB

english, 2016

41

TWO HUMAN X-AUTOSOME TRANSLOCATIONS IDENTIFIED BY AUTORADIOGRAPHY AND FLUORESCENCE

COHEN, MAIMON M., LIN, CHYI-CHYANG, SYBERT, VIRGINIA, ORECCHIO, EDWARD J.

Journal:

Obstetric and Gynecologic Survey

Year:

1973

File:

PDF, 274 KB

1973