1. Abnormal brain magnetic resonance imaging in two patients with Smith–Magenis syndrome. Issue 8 (30th April 2014) Authors: Maya, Idit; Vinkler, Chana; Konen, Osnat; Kornreich, Liora; Steinberg, Tamar; Yeshaya, Josepha; Latarowski, Victoria; Shohat, Mordechai; Lev, Dorit; Baris, Hagit N. Journal: American journal of medical genetics Issue: Volume 164:Issue 8(2014.) Page Start: 1940 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome. Issue 1 (30th September 2013) Authors: Baris, Hagit N.; Chan, Wai‐Man; Andrews, Caroline; Behar, Doron M.; Donovan, Diana J.; Morton, Cynthia C.; Ranells, Judith; Pal, Tuya; Ligon, Azra H.; Engle, Elizabeth C. Journal: Clinical case reports Issue: Volume 1:Issue 1(2013:Oct.) Page Start: 30 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity. Issue 3 (6th November 2015) Authors: Baris, Hagit N.; Barnes‐Kedar, Inbal; Toledano, Helen; Halpern, Marisa; Hershkovitz, Dov; Lossos, Alexander; Lerer, Israela; Peretz, Tamar; Kariv, Revital; Cohen, Shlomi; Half, Elizabeth E.; Magal, Nurit; Drasinover, Valerie; Wimmer, Katharina; Goldberg, Yael; Bercovich, Dani; Levi, Zohar Journal: Pediatric blood & cancer Issue: Volume 63:Issue 3(2016) Page Start: 418 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Correspondence on "Neurocutaneous Syndromes and Brain Tumors". (June 2016) Authors: Toledano, Helen; Barnes-Kedar, Inbal; Baris, Hagit N. Journal: Journal of child neurology Issue: Volume 31:Number 7(2016:Jul.) Page Start: 944 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Is one diagnosis the whole story? patients with double diagnoses. Issue 9 (8th June 2016) Authors: Kurolap, Alina; Orenstein, Naama; Kedar, Inbal; Weisz Hubshman, Monika; Tiosano, Dov; Mory, Adi; Levi, Zohar; Marom, Daphna; Cohen, Lior; Ekhilevich, Nina; Douglas, Jessica; Nowak, Catherine Bearce; Tan, Wen‐Hann; Baris, Hagit N. Journal: American journal of medical genetics Issue: Volume 170:Issue 9(2016) Page Start: 2338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Outcome of pregnancies in women receiving velaglucerase alfa for Gaucher disease. Issue 4 (26th February 2014) Authors: Elstein, Deborah; Hughes, Derralynn; Goker‐Alpan, Ozlem; Stivel, Miriam; Baris, Hagit N.; Cohen, Ian J.; Granovsky‐Grisaru, Sorina; Samueloff, Arnon; Mehta, Atul; Zimran, Ari Journal: Journal of obstetrics and gynaecology research Issue: Volume 40:Issue 4(2014:Apr.) Page Start: 968 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance. Issue 25 (1st September 2021) Authors: Durno, Carol; Ercan, Ayse Bahar; Bianchi, Vanessa; Edwards, Melissa; Aronson, Melyssa; Galati, Melissa; Atenafu, Eshetu G.; Abebe-Campino, Gadi; Al-Battashi, Abeer; Alharbi, Musa; Azad, Vahid Fallah; Baris, Hagit N.; Basel, Donald; Bedgood, Raymond; Bendel, Anne; Ben-Shachar, Shay; Blumenthal, De... Journal: Journal of clinical oncology Issue: Volume 39:Issue 25(2021) Page Start: 2779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗