Chyi-Chyang Lin

Chyi-Chyang Lin

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Chyi-Chyang Lin

Chyi-Chyang Lin

Publications by authors named "Chyi-Chyang Lin"

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34Publications

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Hematopoietically expressed homeobox gene is associated with type 2 diabetes in KK Cg-A/J mice and a Taiwanese Han Chinese population.

Exp Ther Med 2018 Jul 10;16(1):185-191. Epub 2018 May 10.

Human Genetics Center, Department of Medical Research, China Medical University Hospital, China Medical University, Taichung 40447, Taiwan, R.O.C.

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http://dx.doi.org/10.3892/etm.2018.6152DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995076PMC
July 2018

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

J Formos Med Assoc 2015 Jan 8;114(1):81-7. Epub 2012 Mar 8.

Department of Medical Research, China Medical University and Hospital, Taichung, Taiwan; Graduate Institute of Basic Medical Sciences, China Medical University and Hospital, Taichung, Taiwan. Electronic address:

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http://dx.doi.org/10.1016/j.jfma.2011.05.015DOI Listing
January 2015

Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract.

Pediatr Neonatol 2013 Apr 8;54(2):132-6. Epub 2012 Dec 8.

Division of Pediatric Neurology, Children's Medical Center, China Medical University Hospital, Taichung, Taiwan.

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http://dx.doi.org/10.1016/j.pedneo.2012.10.010DOI Listing
April 2013

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.

Am J Med Genet A 2010 Jul;152A(7):1862-7

Department of Obstetrics and Gynecology, China Medical University Hospital, Taichung, Taiwan.

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http://dx.doi.org/10.1002/ajmg.a.33452DOI Listing
July 2010

Complex genomic organization of Indian muntjac centromeric DNA.

Chromosome Res 2009 18;17(8):1051-62. Epub 2009 Nov 18.

Department of Agronomy, National Chung Hsing University, Taichung, 402, Taiwan.

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http://dx.doi.org/10.1007/s10577-009-9097-zDOI Listing
April 2010

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

Am J Med Genet A 2009 Dec;149A(12):2768-74

Department of Obstetrics and Gynecology, Chia-Yi Veterans Hospital, Chai-Yi, Taiwan.

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http://dx.doi.org/10.1002/ajmg.a.32878DOI Listing
December 2009

Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX male.

Am J Med Genet A 2009 Dec;149A(12):2775-81

Department of Obstetrics and Gynecology, China Medical University Hospital, Taichung, Taiwan.

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http://doi.wiley.com/10.1002/ajmg.a.32958
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http://dx.doi.org/10.1002/ajmg.a.32958DOI Listing
December 2009

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

Prenat Diagn 2009 Nov;29(11):1058-60

Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

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http://dx.doi.org/10.1002/pd.2332DOI Listing
November 2009

Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.

Taiwan J Obstet Gynecol 2009 Sep;48(3):292-5

Department of Obstetrics and Gynecology, China Medical University Hospital, Taichung, Taiwan.

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http://dx.doi.org/10.1016/S1028-4559(09)60307-7DOI Listing
September 2009

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

Fertil Steril 2006 Nov;86(5):1514.e1-2

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan.

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http://dx.doi.org/10.1016/j.fertnstert.2006.02.127DOI Listing
November 2006

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

Am J Med Genet A 2006 Jul;140(14):1594-600

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.

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http://dx.doi.org/10.1002/ajmg.a.31329DOI Listing
July 2006

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

Am J Med Genet A 2005 Dec;139A(2):146-50

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.

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http://dx.doi.org/10.1002/ajmg.a.30997DOI Listing
December 2005

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

Prenat Diagn 2005 Feb;25(2):112-8

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.

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http://dx.doi.org/10.1002/pd.1083DOI Listing
February 2005

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

Prenat Diagn 2004 Oct;24(10):767-73

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.

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http://dx.doi.org/10.1002/pd.977DOI Listing
October 2004

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

Eur J Hum Genet 2002 Aug;10(8):495-8

Department of Life Sciences and Genetics Laboratory, Chung Shan Medical University, Taichung, Taiwan, Republic of China.

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http://www.nature.com/articles/5200838
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http://dx.doi.org/10.1038/sj.ejhg.5200838DOI Listing
August 2002