Whole-exome sequencing in fetuses with central nervous system abnormalities by Reches, Adi, Hiersch, Liran, Simchoni, Sharon, Barel, Dalit, Greenberg, Rotem, Ben Sira, Liat, Malinger, Gustavo, Yaron, Yuval

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160: Chromosomal microarray for patient choice disadvantage may outweigh benefit by Brabbing-Goldstein, Dana, Reches, Adi, Shira, Anat Bar, Yaron, Yuval

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Gonadotropin-Releasing Hormone Agonist Versus Recombinant Human Chorionic Gonadotropin Triggering in Fertility Preservation Cycles by Herzberger, Einat Haikin, Knaneh, Sabaa, Amir, Hadar, Reches, Adi, Ben-Yosef, Dalit, Kalma, Yael, Azem, Foad, Samara, Nivin

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9234 A Case of Gigantism Due to An AIP Gene Mutation: Implications for Genetic Counseling and Preimplantation Genetic Diagnosis by Serebro, Merav, Bach, Michal Yacobi, Zohar, Naomi Even, Reches, Adi, Greenman, Yona

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Association of aberrant right subclavian artery with abnormal karyotype and microarray results by Svirsky, Ran, Reches, Adi, Brabbing‐Goldstein, Dana, Bar‐Shira, Anat, Yaron, Yuval

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Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations by Amir, Hadar, Barbash-Hazan, Shiri, Kalma, Yael, Frumkin, Tsvia, Malcov, Mira, Samara, Nivin, Hasson, Joseph, Reches, Adi, Azem, Foad, Ben-Yosef, Dalit

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Microarray analysis in pregnancies with isolated unilateral kidney agenesis by Sagi-Dain, Lena, Maya, Idit, Peleg, Amir, Reches, Adi, Banne, Ehud, Baris, Hagit N, Tenne, Tamar, Singer, Amihood, Ben-Shachar, Shay

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Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model-a pilot study by Michaelson-Cohen, Rachel, Salzer, Liat Sheelo, Brabbing-Goldstein, Dana, Yaron, Yuval, Reches, Adi, Yonath, Hagith, Regev, Miriam, Shani, Hagit, Altarescu, Gheona, Segel, Reeval, Sukenik-Halevy, Rivka, Daum, Hagit, Harel, Tamar, Meiner, Vardiella, Basel-Salmon, Lina, Sagi-Dain, Lena, Maya, Idit

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257: The added value of whole exome sequencing (WES) in fetuses with structural abnormalities by Hiersch, Liran, Reches, Adi, Simchoni, Sharon, Barel, Dalit, Greenberg, Rotem, Yaron, Yuval

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Blastomere biopsy for PGD delays embryo compaction and blastulation: a time-lapse microscopic analysis by Bar-El, Liron, Kalma, Yael, Malcov, Mira, Schwartz, Tamar, Raviv, Shaul, Cohen, Tania, Amir, Hadar, Cohen, Yoni, Reches, Adi, Amit, Ami, Ben-Yosef, Dalit

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Identification of novel microRNAs regulating HLA-G expression and investigating their clinical relevance in renal cell carcinoma by Jasinski-Bergner, Simon, Reches, Adi, Stoehr, Christine, Massa, Chiara, Gonschorek, Evamaria, Huettelmaier, Stefan, Braun, Juliane, Wach, Sven, Wullich, Bernd, Spath, Verena, Wang, Ena, Marincola, Francesco M, Mandelboim, Ofer, Hartmann, Arndt, Seliger, Barbara

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Complex chromosomal rearrangement—a lesson learned from PGS by Frumkin, Tsvia, Peleg, Sagit, Gold, Veronica, Reches, Adi, Asaf, Shiri, Azem, Foad, Ben-Yosef, Dalit, Malcov, Mira

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NK-92 cells retain vitality and functionality when grown in standard cell culture conditions by Rebecca Kotzur, Alexandra Duev-Cohen, Inbal Kol, Adi Reches, Ofer Mandelboim, Natan Stein

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Association of aberrant right subclavian artery with abnormal karyotype and microarray results: The association of ARSA and chromosomal abnormalities by Svirsky, Ran, Reches, Adi, Brabbing-Goldstein, Dana, Bar-Shira, Anat, Yaron, Yuval

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Cover Image, Volume 37, Issue 8 by Svirsky, Ran, Reches, Adi, Brabbing-Goldstein, Dana, Bar-Shira, Anat, Yaron, Yuval

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Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the HNF1B gene by Cleper, Roxana, Reches, Adi, Shapira, Dana, Simchoni, Sharon, Reisman, Lewis, Ben-Sira, Liat, Yaron, Yuval, Wolman, Igal, Malinger, Gustavo, Brabbing-Goldstein, Dana, Ben-Shachar, Shay

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Mass effect: four months after a failed pregnancy, the patient was fatally ill by Grisaru, Dan, Reches, Adi, Nimrod, Adi

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Four months after a failed pregnancy, the patient was fatally ill by GRISARU, Dan, RECHES, Adi, NIMROD, Adi

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Microscopic chromosome Xp distal deletions - a challenging issue in prenatal genetic counseling by Sukenik-Halevy, Rivka, Reches, Adi, Bar-Shira, Anat, Simchoni, Sharon, Goldstein, Myriam, Orr-Ortreger, Avi, Yaron, Yuval, Ben-Shachar, Shay

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Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance‐Horan syndrome in the extended family by Reches, Adi, Yaron, Yuval, Burdon, Kathryn, Crystal‐Shalit, Ornit, Kidron, Dvora, Malcov, Mira, Tepper, Ron

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