J. Chang

D. Tarng, T. Huang, J. Chang, 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Analysis of ras gene mutations in gastrointestinal cancers.

J. Chang, C. Shen, K. Y. Lin, 1991, Journal of the Formosan Medical Association = Taiwan yi zhi.

Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations

T. Y. Yang, J. Chang, C. Tsai, 2000, Annals of Hematology.

Rapid detection of a recombinant hotspot associated with Charcot-Marie-Tooth disease type IA duplication by a PCR-based DNA test.

Y. Jong, J. Chang, C. P. Chang, 1998, Clinical chemistry.

Aberrant FHIT transcripts in acute myeloid leukaemia

J. Chang, Tyen‐Po Chen, P. Lin, 1997, British journal of haematology.

Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer.

J. Chang, C. P. Chang, C. Tsai, 2000, Gynecologic oncology.

Preliminary evidence for an association of Epstein-Barr virus with pre-ulcerative oral lesions in patients with recurrent aphthous ulcers or Behçet's disease.

C. Chiang, J. Chang, A. Sun, 2007, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract.

M. Kao, T. Y. Yang, J. Chang, 1999, European journal of cancer.

The Promoter Region of the CTLA4 Gene is Associated with Type 1 Diabetes Mellitus

Y. J. Lee, F. Lo, T. Y. Yang, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia

Jan-Gowth Chang, J. Chang, Tyen‐Po Chen, 2000, American journal of hematology.

Glucose-6-phosphate dehydrogenase deficiency.

J. Chang, T. C. Liu, T. Liu, 1995, Critical reviews in oncology/hematology.

Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction

P. H. Chen, J. Chang, S. Chiou, 2005, Annals of Hematology.

Ras oncogene and p53 gene hotspot mutations in colorectal cancers

P. H. Chen, J. Chang, S. Y. Lin, 1995, Journal of gastroenterology and hepatology.

No association of alpha-2 macroglobulin gene five-nucleotide deletion with AD in Taiwan Chinese

J. Chang, C. Tsai, W. Hsu, 1999, Neurology.

Prenatal prediction of spinal muscular atrophy in Chinese

Hung Li, Y. Jong, H. Hsieh-Li, 1999, Prenatal diagnosis.

Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population.

J. Chang, Ta‐Chih Liu, T. C. Liu, 1997, Blood.

Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.

T. Tang, P. H. Chen, J. Chang, 1992, Blood.

Molecular basis of spinal muscular atrophy in Chinese.

Y. Jong, T. Y. Yang, J. Chang, 1995, American journal of human genetics.

Human cytomegalovirus as a potential etiologic agent in recurrent aphthous ulcers and Behçet's disease.

C. Chiang, J. Chang, Bu-Yuan Liu, 1996, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

No evidence of correlation between mutation at codon 531 of src and the risk of colon cancer in Chinese.

K. Yeh, J. Chang, C. Tsai, 2000, Cancer letters.

Random amplified polymorphic DNA polymerase chain reaction (RAPD PCR) fingerprints in forensic species identification.

J. C. Lee, Jan-Gowth Chang, J. Chang, 1994, Forensic science international.

Rapid detection of −α4.2 deletion of α-thalassemia-2 by polymerase chain reaction

J. Chang, S. Chiou, Ta‐Chih Liu, 1994, Annals of Hematology.

HLA-DMA and DMB genotyping in patients with rheumatoid arthritis.

J. Yen, J. Chang, W. Tsai, 1997, The Journal of rheumatology.

Molecular basis and haematological characterization of β‐thalassaemia major in Taiwan, with a mutation of IVS‐1 3’end TAG → GAG in a Chinese patient

P. H. Chen, J. Chang, S. Chiou, 1993, British journal of haematology.

Hb Köln [beta98(FG5)Val-->Met]: the first case found in a Chinese family.

J. Chang, K. Tsan, L. Perng, 1998, Hemoglobin.

Molecular basis of beta-thalassemia minor in Taiwan.

P. H. Chen, J. Chang, S. Chiou, 1994, International journal of hematology.

Mutation analysis of the ras gene in myelocytic leukemia by polymerase chain reaction and oligonucleotide probes.

J. Chang, H. W. Liu, T. C. Liu, 1991, Journal of the Formosan Medical Association = Taiwan yi zhi.

The screening of 13 short tandem repeat loci in the Chinese population.

L. Tsai, A. Linacre, J. C. Lee, 1997, Forensic science international.

ABO genotyping by mutagenically separated polymerase chain reaction.

L. Tsai, J. C. Lee, J. Chang, 1996, Forensic science international.

Analysis of aberrant transcription of TSG101 in hepatocellular carcinomas.

P. H. Chen, J. Chang, S. Y. Lin, 1999, European journal of cancer.

Aberrant FHIT transcripts in hepatocellular carcinomas.

P. H. Chen, J. Chang, Y. J. Chen, 1998, British Journal of Cancer.

Rapid detection of hemoglobin variants by mutagenically separate polymerase chain reaction (MS-PCR)

J. Chang, H. J. Liu, J. M. Huang, 1995, Annals of Hematology.

ABO genotyping by polymerase chain reaction.

J. C. Lee, J. Chang, 1992, Journal of forensic sciences.

Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.

H. Chao, F. Tsai, Chang-Hai Tsai, 2000, Clinical chemistry.

Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese.

H. Chao, Y. J. Lee, J. Chang, 2000, The Journal of clinical endocrinology and metabolism.

Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites.

P. H. Chen, J. Chang, S. Chiou, 1992, Blood.

Eosinophilic gastroenteritis with eosinophilic ascites: report of a case.

J. Chang, C. Siauw, P. H. Chen, 1990, Journal of the Formosan Medical Association = Taiwan yi zhi.

Rapid molecular diagnosis of hemoglobin variants by RT-PCR of reticulocyte mRNA and direct sequencing.

P. H. Chen, J. Chang, T. C. Liu, 1992, Hemoglobin.

Human RhDel is caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene.

J. Chang, K. Tsan, C. Peng, 1998, Blood.

Resistance to recombinant erythropoietin in a hemodialysis patient with heterozygous hemoglobinopathy J-Meinung.

D. Tarng, T. Huang, J. Chang, 1997, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Hb Kaohsiung or New York: a T----A substitution at codon 113 of the beta-globin chain creates an Alu I cutting site.

P. H. Chen, J. Chang, L. S. Lee, 1992, Hemoglobin.

Gene frequencies of the HPA-1 to HPA-13, Oe and Gov platelet antigen alleles in Taiwanese, Indonesian, Filipino and Thai populations.

J. Chang, C. Chen, I.-L. Lin, 2003, International journal of molecular medicine.

Gene frequencies of the HPA-1 to HPA-8w platelet antigen alleles in Taiwanese, Indonesian, and Thai

C. Lin, J. Chang, Cailu Lin, 2002, Annals of Hematology.

Hb Owari associated with aα-thalassaemia-1 in a Taiwanese subject

J. Chang, T. Er, L. Hsieh, 2009, British journal of biomedical science.

Molecular diagnosis of thalassemia in Taiwan.

J. Chang, H. J. Liu, 1995, Gaoxiong yi xue ke xue za zhi = The Kaohsiung journal of medical sciences.

Clonal analysis in acute myeloid leukemia by polymerase chain reaction.

J. Chang, S. Hwang, T. C. Liu, 1995, Gaoxiong yi xue ke xue za zhi = The Kaohsiung journal of medical sciences.

Molecular characterization of Hb H disease by polymerase chain reaction.

J. Chang, C. Tsao, S. Chiou, 1993, Acta haematologica.

Rapid diagnosis of hemoglobin constant spring and hemoglobin E by amplified created restriction sites.

P. H. Chen, J. Chang, T. C. Liu, 1993, Blood.

Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.

P. H. Chen, J. Chang, L. S. Lee, 1992, International journal of hematology.

Hb Siriraj: a G-->A substitution at codon 7 of the beta-globin chain creates an MboII cutting site.

J. Chang, C. Peng, C. Tsai, 1999, Hemoglobin.

Detection of beta-globin gene from single hairs.

J. Chang, H. W. Liu, T. C. Liu, 1990, Gaoxiong yi xue ke xue za zhi = The Kaohsiung journal of medical sciences.

Infectivity in asymptomatic hepatitis B carriers: its correlation with HBeAg/anti-HBe status.

J. Chang, K. Choo, P. H. Chen, 1989, Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association.

Mutation analysis of PTEN/MMAC 1 in sporadic thyroid tumors.

S. Shin, M. Hsieh, J. Chang, 2000, The Kaohsiung journal of medical sciences.

Rapid genotyping of ABO blood group.

J. C. Lee, P. H. Chen, J. Chang, 1992, Blood.

P53 codon 72Arg polymorphism is not a risk factor for carcinogenesis in the chinese.

K. Yeh, J. Chang, C. Tsai, 1999, International journal of molecular medicine.

Genetic analysis of interleukin-10 promoter region in patients with systemic lupus erythematosus in Taiwan.

T. Ou, J. Yen, J. Chang, 1998, The Kaohsiung journal of medical sciences.

Rapid diagnosis of alpha-thalassemia-1 of southeast Asia type and hydrops fetalis by polymerase chain reaction.

P. H. Chen, J. Chang, L. S. Lee, 1991, Blood.

"Hot spots" mutation analysis of p53 gene in gastrointestinal cancers by amplification of naturally occurring and artificially created restriction sites.

P. H. Chen, J. Chang, S. Y. Lin, 1993, Clinical chemistry.

Cloning and characterization of a human beta,beta-carotene-15,15'-dioxygenase that is highly expressed in the retinal pigment epithelium.

P. Campochiaro, D. Zack, J. Chang, 2001, Genomics.

[Current clinical approaches and gene mutation study of beta-thalassemia major].

J. Chang, S. Tsai, J. Sheen, 1995, Gaoxiong yi xue ke xue za zhi = The Kaohsiung journal of medical sciences.

Are aberrant transcripts of FHIT, TSG101, and PTEN/MMAC1 oncogenesis related?

J. Chang, N. M. Wang, 1999, International Journal of Molecular Medicine.

Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells.

F. Tsai, J. Chang, C. Peng, 2000, International Journal of Oncology.

A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese.

J. Chang, S. Chiou, L. Perng, 1992, Human Molecular Genetics.

Molecular characterization of glucose‐6‐phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinaemia

J. Chang, B. H. Chen, S. Chiou, 1994, British journal of haematology.

Sequence polymorphism of mitochondrial D-loop DNA in the Taiwanese Han population.

L. Tsai, A. Linacre, J. C. Lee, 2001, Forensic science international.

Molecular characterization of secretor type α(1,2)-fucosyltransferase gene deficiency in the Philippine population

M. Kao, J. Chang, C. Peng, 1999, Annals of Hematology.

Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data.

F. Tsai, J. Chang, J. Y. Wu, 1999, American journal of medical genetics.

Mutation analysis of K-ras oncogenes in gastroenterologic cancers by the amplified created restriction sites method.

J. Chang, S. Y. Lin, C. Siauw, 1993, American journal of clinical pathology.