A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome von Yin, Y, Liu, X-H, Li, X-H, Fan, N, Lei, D-F, Wang, Y, Cai, S-P, Zhou, X-M, Chen, X-M, Liu, X-Y

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Association of the genetic polymorphisms of NFKB1 with susceptibility to ovarian cancer von Chen, L P, Cai, P S, Liang, H B

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Rapid and Simultaneous Typing of Hemoglobin S, Hemoglobin C, and Seven Mediterranean β-Thalassemia Mutations by Covalent Reverse Dot-Blot Analysis: Application to Prenatal Diagnosi... von Maggio, A., Giambona, A., Cai, S.P., Wall, J., Kan, Y.W., Chehab, F.F.

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A novel NF1 frame-shift mutation (c.702_703delGT) in a Chinese family with neurofibromatosis type 1 von Cai, S P, Fan, N, Chen, J, Xia, Z L, Wang, Y, Zhou, X M, Yin, Y, Wen, T L, Xia, Q J, Liu, X Y, Wang, H Y

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Study on the dynamic changes of D-dimer during pregnancy and early puerperium von Xu, D, Cai, S P, Xu, J W, Liang, C, He, J

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β-thalassemia mutations in Indonesia and their linkage to β haplotypes von LIE-INJO, L. E, CAI, S.-P, WAHIDIJAT, I, MOESLICHAN, S, LIM, M. L, EVANGELISTA, L, DOHERTY, M, KAN, Y. W

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A Short-Term Trial of Butyrate to Stimulate Fetal-Globin-Gene Expression in the β-Globin Disorders von Perrine, Susan P, Ginder, Gordon D, Faller, Douglas V, Dover, George H, Ikuta, Tohru, Witkowska, H. Ewa, Cai, Shi-ping, Vichinsky, Elliott P, Olivieri, Nancy F

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Two Novel β-Thalassemia Mutations in the 5’ and 3’ Noncoding Regions of the β-Globin Gene von Cai, Shi-Ping, Eng, Barry, Francombe, William H., Olivieri, Nancy F., Kendall, Alan G., Waye, John S., Chui, David H.K.

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Rapid Prenatal Diagnosis of β Thalassemia Using DNA Amplification and Nonradioactive Probes von Cai, S.-P., Chang, C.A., Zhang, J.-Z., Saiki, R.K., Erlich, H.A., Kan, Y.W.

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Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks von Cai, S P, Wall, J, Kan, Y W, Chehab, F F

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A new TATA box mutation detected at prenatal diagnosis for β-thalassemia von SHI-PING CAI, JI-ZENG ZHANG, DOHERTY, M, YUET WAI KAN

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Characterization of intraocular pressure responses of the Tibetan monkey (Macaca thibetana) von Liu, Guo, Zeng, Tao, Yu, Wenhan, Yan, Naihong, Wang, Hongxing, Cai, Su-ping, Pang, Iok-Hou, Liu, Xuyang

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Sequence analysis of MYOC and CYP1B1 in a Chinese pedigree of primary open-angle glaucoma von Chen, Jun, Cai, Su-ping, Yu, Wenhan, Yan, Naihong, Tang, Li, Chen, Xiaoming, Liu, Xuyang

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Molecular genetics of familial nystagmus complicated with cataract and iris anomalies von Yan, Naihong, Zhao, Yongwang, Wang, Yun, Xie, Airui, Huang, Haitao, Yu, Wenhan, Liu, Xuyang, Cai, Su-ping

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A novel MYOC heterzygous mutation identified in a Chinese Uygur pedigree with primary open-angle glaucoma von Cai, S-P, Muhemaiti, P, Yin, Y, Cheng, H, Di Ya, A, Keyimu, M, Cao, X, Fan, N, Jiang, L, Yan, N, Zhou, X, Wang, Y, Liu, X

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Identification of the multiple β-thalassemia mutations by denaturing gradient gel electrophoresis von Cai, S P, Kan, Y W

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Equivalent Wheel Load Approach for Slender Cable-Stayed Bridge Fatigue Assessment under Traffic and Wind: Feasibility Study von Chen, S. R, Cai, C. S

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High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region von Waye, J S, Cai, S P, Eng, B, Clark, C, Adams, 3rd, J G, Chui, D H, Steinberg, M H

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A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion : application to β-thalassemia von SHI-PING CAI, ENG, B, YUET WAI KAN, CHUI, D. H. K

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Molecular basis of β thalassemia in South China: strategy for DNA analysis von JI-ZENG ZHANG, SHI-PING CAI, XING HE, HUAN-XIN LIN, HUA-JIN LIN, ZHI-GUANG HUANG, CHEHAB, F. F, YUET WAI KAN

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