Hakutulokset - Dietrich, Jennifer E.

MicroRNAs and Recent Insights into Pediatric Ovarian Cancers Tekijä Francis, Jessica C., Kolomeyevskaya, Nonna, Mach, Claire M., Dietrich, Jennifer E., Anderson, Matthew L.

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A genome-wide screen for copy number alterations in an adolescent pilot cohort with Müllerian anomalies Tekijä Murry, Jaclyn B., Santos, Xiomara, Wang, Xiaoling, Wan, Ying-Wooi, Van den Veyver, Ignatia B., Dietrich, Jennifer E.

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Intrauterine growth restriction and hypospadias: is there a connection? Tekijä Chen, Min-Jye, Macias, Charles G, Gunn, Sheila K, Dietrich, Jennifer E, Roth, David R, Schlomer, Bruce J, Karaviti, Lefkothea P

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Assessing sex assignment concordance with genotype and phenotype Tekijä Suresh, Deepa, Crawford, Jessica, Axelrad, Marni E, Gunn, Sheila K, McCullough, Laurence, Smith, O’ Brian, Sutton, Vernon R, Roth, David, Karaviti, Lefkothea P, Dietrich, Jennifer E

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The spectrum and severity of bleeding in adolescents with low von Willebrand factor–associated heavy menstrual bleeding Tekijä Srivaths, Lakshmi, Minard, Charles G., O’Brien, Sarah H., Wheeler, Allison P., Mullins, Eric, Sharma, Mukta, Sidonio, Robert, Jain, Shilpa, Zia, Ayesha, Ragni, Margaret V., Kulkarni, Roshni, Dietrich, Jennifer E., Kouides, Peter A.

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Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team Tekijä Douglas, Ganka, Axelrad, Marni E., Brandt, Mary L., Crabtree, Elizabeth, Dietrich, Jennifer E., French, Shannon, Gunn, Sheila, Karaviti, Lefkothea, Lopez, Monica E., Macias, Charles G., McCullough, Laurence B., Suresh, Deepa, Sutton, V. Reid

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State of the art review in gonadal dysgenesis: challenges in diagnosis and management Tekijä McCann-Crosby, Bonnie, Mansouri, Roshanak, Dietrich, Jennifer E, McCullough, Laurence B, Sutton, V Reid, Austin, Elise G, Schlomer, Bruce, Roth, David R, Karaviti, Lefkothea, Gunn, Sheila, Hicks, M John, Macias, Charles G

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Pediatric Medical Device Development by Surgeons via Capstone Engineering Design Programs Tekijä Sack, Bryan S., Elizondo, Rodolfo A., Huang, Gene O., Janzen, Nicolette, Espinoza, Jimmy, Sanz-Cortes, Magdalena, Dietrich, Jennifer E., Hakim, Julie, Richardson, Eric, Oden, Maria, Hanks, John, Haridas, Balakrishna, Hury, James F., Koh, Chester J.

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Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations Tekijä Sadler, Brooke, Minard, Charles G., Haller, Gabe, Gurnett, Christina A., O’Brien, Sarah H., Wheeler, Allison, Jain, Shilpa, Sharma, Mutka, Zia, Ayesha, Kulkarni, Roshni, Mullins, Eric, Ragni, Margaret V., Sidonio, Robert, Dietrich, Jennifer E., Kouides, Peter A., Di Paola, Jorge, Srivaths, Lakshmi

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Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome Tekijä Chen, Na, Zhao, Sen, Jolly, Angad, Wang, Lianlei, Pan, Hongxin, Yuan, Jian, Chen, Shaoke, Koch, André, Ma, Congcong, Tian, Weijie, Jia, Ziqi, Kang, Jia, Zhao, Lina, Qin, Chenglu, Fan, Xin, Rall, Katharina, Coban-Akdemir, Zeynep, Chen, Zefu, Jhangiani, Shalini, Liang, Ze, Niu, Yuchen, Li, Xiaoxin, Yan, Zihui, Wu, Yong, Dong, Shuangshuang, Song, Chengcheng, Qiu, Guixing, Zhang, Shuyang, Liu, Pengfei, Posey, Jennifer E., Zhang, Feng, Luo, Guangnan, Wu, Zhihong, Su, Jianzhong, Zhang, Jianguo, Chen, Eugenia Y., Rouskas, Konstantinos, Glentis, Stavros, Bacopoulou, Flora, Deligeoroglou, Efthymios, Chrousos, George, Lyonnet, Stanislas, Polak, Michel, Rosenberg, Carla, Dingeldein, Irene, Bonilla, Ximena, Borel, Christelle, Gibbs, Richard A., Dietrich, Jennifer E., Dimas, Antigone S., Antonarakis, Stylianos E., Brucker, Sara Y., Lupski, James R., Wu, Nan, Zhu, Lan

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