Yueh‐Chun Li

发表

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, S. Chern, Shuan-Pei Lin, 2005, Prenatal diagnosis.

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

F. Tsai, M. Ho, Wei‐De Lin, 2009, American journal of medical genetics. Part A.

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

F. Tsai, Chang-Hai Tsai, Y. Hsieh, 2006, Prenatal diagnosis.

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

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, American journal of medical genetics. Part A.

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, S. Chern, Shuan-Pei Lin, 2005, Prenatal diagnosis.

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, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

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

Erwin G. Van Meir, C. Tzeng, Jin H. Song, 2006, Clinical Cancer Research.

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

Chih-ping Chen, S. Chern, Wayseen Wang, 2006, Prenatal diagnosis.

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

Chih-ping Chen, Wayseen Wang, Chen‐Chi Lee, 2006, Fertility and sterility.

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

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, American journal of medical genetics. Part A.

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

Ya-Ming Cheng, Yi-Chun Wang, Chyi-chyang Lin, 2014, Zoological Studies.

Construction of an Indian Muntjac BAC Library and Production of the Most Highly Dense FISH Map of the Species

Ya-Ming Cheng, Chyi-chyang Lin, L. Hsieh, 2008 .

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

Charles Lee, D. Sanoudou, Shuan-yow Li, 2004, Chromosome Research.

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

F. Tsai, S. Setlur, S. Chien, 2015, Journal of the Formosan Medical Association = Taiwan yi zhi.

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

K. Chao, K. Wen, Chia-Ming Chang, 2009, American journal of medical genetics. Part 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

Ling-Hui Li, Jer-Yuarn Wu, S. Chien, 2010, American journal of medical genetics. Part A.

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

F. Tsai, Chyi-chyang Lin, Yueh-Chun Li, 2015, Genes & Genomics.

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

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, Prenatal diagnosis.

Partial trisomy 3p and monosomy 7p associated with tetralogy of Fallot and infantile seizure.

K. Chao, Chih-ping Chen, Pi‐Chang Lee, 2007, Taiwanese journal of obstetrics & gynecology.

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

Chih-ping Chen, C. Tzen, S. Chern, 2004, Prenatal diagnosis.

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

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, Prenatal diagnosis.

Complex genomic organization of Indian muntjac centromeric DNA

Ya-Ming Cheng, Chyi-chyang Lin, L. Hsieh, 2009, Chromosome Research.

Sumoylation of p45/NF-E2: Nuclear Positioning and Transcriptional Activation of the Mammalian β-Like Globin Gene Locus

Chun-Yuan Ting, C. Shen, S. Wen, 2005, Molecular and Cellular Biology.

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.

K. Chao, Peng-Hui Wang, K. Wen, 2012, Taiwanese journal of obstetrics & gynecology.

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, Wayseen Wang, 2005, Prenatal diagnosis.

Novel point mutation within intron 10 of FMR‐1 gene causing fragile X syndrome

Shuan-yow Li, Shio‐Jean Lin, Yueh‐Chun Li, 1997, Human mutation.

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, Wayseen Wang, Tung-Yao Chang, 2006, Prenatal diagnosis.

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

F. Tsai, Chyi-chyang Lin, Yingqiu Pan, 2015, Genes & Genomics.