Publications by authors named "Chyi-Chyang Lin"

Claim this Profile
H
Hematopoietically expressed homeobox gene is associated with type 2 diabetes in KK Cg-A/J mice and a Taiwanese Han Chinese population.
Chi-Cheng Lu, Yng-Tay Chen, Shih-Yin Chen, Yuan-Man Hsu, Chyi-Chyang Lin

Exp Ther Med· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats.
Yueh-Chun Li, Shu-Chin Chien, Sunita R Setlur, Wei-De Lin, Fuu-Jen Tsai, Chyi-Chyang Lin

J Formos Med Assoc· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract.
Yu-Tzu Chang, I-Ching Chou, Chung-Hsing Wang, Zheng-Nan Chin, Huang-Tsung Kuo, Chyi-Chyang Lin

Pediatr Neonatol· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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, Chyi-Chyang Lin

Taiwan J Obstet Gynecol· June 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
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, Wen-Hsiang Lin, Chyi-Chyang Lin

Theriogenology· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Taiwan J Obstet Gynecol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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, Wen-Ling Chen

Taiwan J Obstet Gynecol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
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, Chyi-Chyang Lin

Am J Med Genet A· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Taiwan J Obstet Gynecol· June 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
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

Chromosome Res· April 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
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, Chyi-Chyang Lin

Am J Med Genet A· December 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
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, Chyi-Chyang Lin

Am J Med Genet A· December 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
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

Prenat Diagn· November 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Taiwan J Obstet Gynecol· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional genomic analysis identified epidermal growth factor receptor activation as the most common genetic event in oral squamous cell carcinoma.
Jim Jinn-Chyuan Sheu, Chun-Hung Hua, Lei Wan, Ying-Ju Lin, Ming-Tsung Lai, Chin-Fen Lin, Chyi-Chyang Lin

Cancer Res· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

J Formos Med Assoc· October 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Intragenic microdeletion of RUNX2 is 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

Genomic Med· January 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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, Lin-Chao Chen

Taiwan J Obstet Gynecol· September 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Fertil Steril· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Prenat Diagn· October 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Prenat Diagn· August 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
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

Am J Med Genet A· July 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic alterations in human malignant glioma cells associate with the cell resistance to the combination treatment with tumor necrosis factor-related apoptosis-inducing ligand and chemotherapy.
Yueh-Chun Li, Ching-Cherng Tzeng, Jin H Song, Fuu-Jen Tsia, Lie-Jiau Hsieh, Chyi-Chyang Lin

Clin Cancer Res· May 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Prenat Diagn· April 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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

Prenat Diagn· April 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis