Iron Overload Is Rare in Patients Homozygous for the H63D Mutation von Kelley, Melissa, Joshi, Nikhil, Xie, Yagang, Borgaonkar, Mark

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Individuals homozygous for the H63D mutation have significantly elevated iron indexes von SAMARASENA, Jason, WINSOR, Wendy, LUSH, Richard, DUGGAN, Peter, YAGANG XIE, BORGAONKAR, Mark

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Concordance of BAI and BMI with DXA in the Newfoundland Population von Sun, Guang, Cahill, Farrell, Gulliver, Wayne, Yi, Yanqing, Xie, Yagang, Bridger, Tracey, Pace, David, Zhang, Hongwei

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Puzzle of the role for the MTHFR C. 677C>T variant and C. 1298A>C in cardiovascular diseases von Xie, Yagang, Cui, Jianxun, Li, Shuo, Xu, Yu-Ming, Randell, Edward, Zou, Liwen, Han, Fei-Yu, Xie, Yagang

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A pharmacogenetic analysis of the Canadian Cancer Trials Group MY.10 clinical trial of maintenance therapy for multiple myeloma von Han, Ming, Murugesan, Alli, Bahlis, Nizar J., Song, Kevin, White, Darrell, Chen, Christine, Seftel, Matthew D., Howsen-Jan, Kang, Reece, Donna, Stewart, Keith, Xie, Yagang, Hay, Annette E., Shepherd, Lois, Djurfeldt, Marina, Zhu, Liting, Meyer, Ralph M., Chen, Bingshu E., Reiman, Tony

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A Pharmacogenetic Study of the NCIC CTG Clinical Trial My.10: Single Nucleotide Polymorphisms, Prognosis, and Predicting Benefit from IMiD® Compound Maintenance Therapy Following A... von Han, Ming, Murugesan, Alli, Bahlis, Nizar J, Song, Kevin, White, Darrell, Chen, Christine, Seftel, Matthew D., Howsen-Jan, Kang, Reece, Donna, Stewart, Keith, Xie, Yagang, Hay, Annette E, Shepherd, Lois, Chen, Bingshu E, Djurfeldt, Marina, Reiman, Tony

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Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients von ROBINSON, W. P, BOTTANI, A, YAGING, X, BALAKRISHMAN, J, BINKERT, F, MÄCHLER, M, PRADER, A, SCHINZEL, A

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Biochemical abnormalities in patients with one or more C282Y or H63D mutations of the HFE gene for hereditary hemochromatosis von Lush, Richard B., Duggan, Peter R., Xie, Yagang, Borgaonkar, Mark R.

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ALLELE-ALLELE INTERACTIONS OF MTHFR GENE VARIANTS, AND USES THEREOF IN PREDICTING DISEASE RISK von YAGANG, XIE

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ALLELE-ALLELE INTERACTIONS OF MTHFR GENE VARIANTS, AND USES THEREOF IN PREDICTING DISEASE RISK von XIE YAGANG

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A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13) (q32.3q33.2) : potential mapping of one disease locus von BOTTANI, A, XIE, Y, BINKERT, F, SCHINZEL, A

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Open set identification technology-based work clothes non-wearing detection method von LIAO CHEN, YANG TIANHUI, LIU ZHIRAN, TIAN CAN, XIE YAGANG, WU HAO

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Power system fine-grained semantic question-answering method, device, equipment, medium and product von HAN TINGYU, TIAN CAN, GU XUCHEN, XIE YAGANG, WU HAO, LI ZHAOYING, MO JIAJUN

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Power grid basic level operation problem reply generation method and device, equipment and storage medium von HAN TINGYU, TIAN CAN, SONG GUIYONG, GU XUCHEN, XIE YAGANG, WU HAO, LI ZHAOYING, MO JIAJUN

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Electric power income prediction method and device, computer equipment and storage medium von HAN TINGYU, TIAN CAN, LI BILANG, SONG GUIYONG, GU XUCHEN, XIE YAGANG, WU HAO, LI ZHAOYING, MO JIAJUN

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A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus von Bottani, Armand, Xie, Yagang, Binkert, Franz, Schinzel, Albert

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Prader-Willi or Angelman syndrome in familial 15q11→q13 deletion of maternal origin? von Schinzel, Albert, Robinson, Wendy P, Bottani, Armand, Yagang, Xie, Prader, Andrea

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Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients von Robinson, Wendy P, Bottani, Armand, Yagang, Xie, Balakrishman, Jaya, Binkert, Franz, Mächler, Marco, Prader, Andrea, Schinzel, Albert

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Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin? von Schinzel, A, Robinson, W P, Bottani, A, Yagang, X, Prader, A

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Medical dressings with X photodevelopment matter on surface and preparation method thereof von LI JIANQUAN, XIE YAGANG

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