A novel homozygous DOCK8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK8 deficiency patient von Liu, Y.‐Q., Zhang, G.‐L., Mo, X.‐H., Wang, B., Wu, F., Chen, J., Luo, H., Zhu, L.‐D., Xu, M.‐Y., Zhou, Q., Cai, Q.‐L., Wang, X.‐L.

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Effect of gestational subclinical hypothyroidism on early neurodevelopment of offspring von Chen, L-M, Chen, Q-S, Jin, G-X, Si, G-X, Zhang, Q, Ye, E-l, Yang, H, Cai, L-Q, Peng, M-M, Lin, Z-Z, Yu, L-C, Zhang, C, Lu, X-M

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Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome von Cai, J., Cai, L.-Q., Hong, Y., Zhu, Y.-S.

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A novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters von STAVROU, S. S, ZHU, Y.-S, CAI, L.-Q, KATZ, M. D, HERRERA, C, DEFILLO-RICART, M, IMPERATO-MCGINLEY, J

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The identification of 5α-reductase-2 and 17β-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred von CAN, S, ZHU, Y.-S, CAI, L.-Q, QI LING, KATZ, M. D, AKGUN, S, SHACKLETON, C. H. L, IMPERATO-MCGINLEY, J

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EFFECTS OF LEUKAEMIA INHIBITORY FACTOR ON EMBRYO IMPLANTATION IN THE MOUSE von Cai, L.Q, Cao, Y.J, Duan, E.K

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Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genes von Li, Q., Liu, L. H., Chang, R. X., Pan, G. B., Chen, G., Gao, M., Cai, L. Q., Wang, P. G., Pimentel, J. D., Pittelkow, M. R., Yang, S., Zhang, X. J.

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A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred von ZHU, Y.-S, CAI, L.-Q, CORDERO, J. J, CANOVATCHEL, W. J, KATZ, M. D, IMPERATO-MCGINLEY, J

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5 alpha-reductase-2 gene mutations in the Dominican Republic von Cai, L Q, Zhu, Y S, Katz, M D, Herrera, C, Baéz, J, DeFillo-Ricart, M, Shackleton, C H, Imperato-McGinley, J

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Effects of Stubble Management on Soil Fertility and Crop Yield of Rainfed Area in Western Loess Plateau, China von Luo, Z. Z., Zhang, R. Z., Huang, G. B., Xie, J. H., Cai, L. Q., Li, G. D., Li, L. L.

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Immunogenicity of polyepitope libraries assembled by epitope shuffling: an approach to the development of chimeric gene vaccination against malaria von Cai, Qi-Liang, Wei, Fang, Lin, Ya-Hui, Shao, Ding-Ding, Wang, Heng

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Association of HLA-DRB1 alleles with keloids in Chinese Han individuals von Lu, W.-S., Zhang, W.-Y., Li, Y., Wang, Z.-X., Zuo, X.-B., Cai, L.-Q., Zhu, F., Wang, J.-F., Sun, L.-D., Zhang, X.-J., Yang, S.

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Mutations in CYP11B1 gene: Phenotype-genotype correlations von Zhu, Yuan-Shan, Cordero, Juan J., Can, Selcuk, Cai, Li-Qun, You, Xueke, Herrera, Cecilia, DeFillo-Ricart, Mariano, Shackleton, Cedric, Imperato-McGinley, Julianne

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Metal Element Doping Graphene for the Oxygen Electrode: A Density Functional Calculation von Cai, L.Q., Zhu, H., Liu, Ye, Jiang, Z.Y., Liu, H.Y., Yu, Z.D.

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Central opioid modulation of fetal cardiovascular function: role of mu- and delta-receptors von Szeto, H. H, Zhu, Y. S, Cai, L. Q

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Paternity by Intrauterine Insemination with Sperm from a Man with 5α-Reductase-2 Deficiency von Katz, Melissa D, Kligman, Isaac, Cai, Li-Qun, Zhu, Yuan-Shan, Fratianni, Carmel M, Zervoudakis, Ioannis, Rosenwaks, Zev, Imperato-McGinley, Julianne

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Cervical spondylotic myelopathy treated by anterior multilevel decompression and fusion: follow-up report of 214 cases von YANG, K. C, LU, X. S, CAI, Q. L, YE, L. X, LU, W. Q

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A novel homozygous DOCK 8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK 8 deficiency patient von Liu, Y.‐Q., Zhang, G.‐L., Mo, X.‐H., Wang, B., Wu, F., Chen, J., Luo, H., Zhu, L.‐D., Xu, M.‐Y., Zhou, Q., Cai, Q.‐L., Wang, X.‐L.

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Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome: Characterisation of an androgen receptor mutatio... von Cai, J., Cai, L.-Q., Hong, Y., Zhu, Y.-S.

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Evaluation of the risk factors of depressive disorders comorbid with obstructive sleep apnea von Cai, Liqiang, Xu, Luoyi, Wei, Lili, Sun, Yi, Chen, Wei

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