Oncologists must act to manage cancer detected through prenatal screening von Turriff, Amy E., Bianchi, Diana W.

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Prenatal DNA Sequencing for Fetal Aneuploidy Also Detects Maternal Cancer: Importance of Timely Workup and Management in Pregnant Women von Turriff, Amy E, Annunziata, Christina M, Bianchi, Diana W

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CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone function von Zein, Wadih M, Jeffrey, Brett G, Wiley, Henry E, Turriff, Amy E, Tumminia, Santa J, Tao, Weng, Bush, Ronald A, Marangoni, Dario, Wen, Rong, Wei, Lisa L, Sieving, Paul A

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Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort von Prasov, Lev, Ullah, Ehsan, Turriff, Amy E., Warner, Blake M., Conley, Julie, Mark, Paul R., Hufnagel, Robert B., Huryn, Laryssa A.

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Variants of LRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy von Faridi, Rabia, Yousaf, Rizwan, Gu, Shoujun, Inagaki, Sayaka, Turriff, Amy E., Pelstring, Keith, Guan, Bin, Naik, Amelia, Griffith, Andrew J., Adadey, Samuel Mawuli, Aboagye, Elvis Twumasi, Awandare, Gordon A., Morell, Robert J., Tsilou, Ekaterini, Noyes, Amanda G., Sulmonte, Laura A. G., Wonkam, Ambroise, Schrauwen, Isabelle, Leal, Suzanne M., Azaiez, Hela, Brewer, Carmen C., Riazuddin, Sheikh, Hufnagel, Robert B., Hoa, Michael, Zein, Wadih M., Dios, J. Karl, Friedman, Thomas B.

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Considerations in multi-gene panel testing in pediatric ophthalmology von Turriff, Amy E., Cukras, Catherine A., Brooks, Brian P., Huryn, Laryssa A.

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Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography von Zein, Wadih M, Falsini, Benedetto, Tsilou, Ekaterina T, Turriff, Amy E, Schultz, Julie M, Friedman, Thomas B, Brewer, Carmen C, Zalewski, Christopher K, King, Kelly A, Muskett, Julie A, Rehman, Atteeq U, Morell, Robert J, Griffith, Andrew J, Sieving, Paul A

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Reply von Turriff, Amy E., Cukras, Catherine A., Brooks, Brian P., Huryn, Laryssa A.

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REPLY von Turriff, Amy E., Cukras, Catherine A., Brooks, Brian P., Huryn, Laryssa A.

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Reply von Turriff, Amy E, Cukras, Catherine A, Brooks, Brian P, Huryn, Laryssa A

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Reply von Turriff, Amy E, Cukras, Catherine A, Brooks, Brian P, Huryn, Laryssa A

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Cone Responses in Usher Syndrome Types 1 and 2 by Microvolt Electroretinography von Zein, W. M., Falsini, B., Tsilou, E. T., Turriff, A. E., Schultz, J. M., Friedman, T. B., Brewer, C. C., Zalewski, C. K., King, K. A., Muskett, J. A., Rehman, A. U., Morell, R. J., Griffith, A. J., Sieving, P. A.

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Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery von Cukras, Catherine, Wiley, Henry E., Jeffrey, Brett G., Sen, H. Nida, Turriff, Amy, Zeng, Yong, Vijayasarathy, Camasamudram, Marangoni, Dario, Ziccardi, Lucia, Kjellstrom, Sten, Park, Tae Kwon, Hiriyanna, Suja, Wright, J. Fraser, Colosi, Peter, Wu, Zhijian, Bush, Ronald A., Wei, Lisa L., Sieving, Paul A.

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Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes von Schultz, Julie M, Bhatti, Rashid, Madeo, Anne C, Turriff, Amy, Muskett, Julie A, Zalewski, Christopher K, King, Kelly A, Ahmed, Zubair M, Riazuddin, Saima, Ahmad, Nazir, Hussain, Zawar, Qasim, Muhammad, Kahn, Shaheen N, Meltzer, Meira R, Liu, Xue Z, Munisamy, Murali, Ghosh, Manju, Rehm, Heidi L, Tsilou, Ekaterini T, Griffith, Andrew J, Zein, Wadih M, Brewer, Carmen C, Riazuddin, Sheikh, Friedman, Thomas B

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Prevalence and psychosocial correlates of depressive symptoms among adolescents and adults with Klinefelter syndrome von Turriff, Amy, Levy, Howard P., Biesecker, Barbara

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