1. A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome. Issue 2 (15th October 2020) Authors: Abe, Keisuke; Dowsett, Leah; Wada, Randal; Hutchins, Kelley Journal: Pediatric blood & cancer Issue: Volume 68:Issue 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cornelia de Lange syndrome in diverse populations. Issue 2 (6th January 2019) Authors: Dowsett, Leah; Porras, Antonio R.; Kruszka, Paul; Davis, Brandon; Hu, Tommy; Honey, Engela; Badoe, Eben; Thong, Meow‐Keong; Leon, Eyby; Girisha, Katta M.; Shukla, Anju; Nayak, Shalini S.; Shotelersuk, Vorasuk; Megarbane, Andre; Phadke, Shubha; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Ferr... Journal: American journal of medical genetics Issue: Volume 179:Issue 2(2019) Page Start: 150 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cornelia de Lange syndrome in diverse populations. Issue 2 (6th January 2019) Authors: Dowsett, Leah; Porras, Antonio R.; Kruszka, Paul; Davis, Brandon; Hu, Tommy; Honey, Engela; Badoe, Eben; Thong, Meow‐Keong; Leon, Eyby; Girisha, Katta M.; Shukla, Anju; Nayak, Shalini S.; Shotelersuk, Vorasuk; Megarbane, Andre; Phadke, Shubha; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Ferr... Journal: American journal of medical genetics Issue: Volume 179:Issue 2(2019) Page Start: 150 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover Image, Volume 176A, Number 5, May 2018. Issue 5 (21st April 2018) Authors: Kruszka, Paul; Porras, Antonio R.; de Souza, Deise Helena; Moresco, Angélica; Huckstadt, Victoria; Gill, Ashleigh D.; Boyle, Alec P.; Hu, Tommy; Addissie, Yonit A.; Mok, Gary T. K.; Tekendo‐Ngongang, Cedrik; Fieggen, Karen; Prijoles, Eloise J.; Tanpaiboon, Pranoot; Honey, Engela; Luk, Ho‐Ming; Lo... Journal: American journal of medical genetics Issue: Volume 176:Issue 5(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Delayed diagnosis and racial bias in children with genetic conditions. Issue 4 (17th January 2022) Authors: Omorodion, Jacklyn; Dowsett, Leah; Clark, Robin D.; Fraser, Jamie; Abu‐El‐Haija, Aya; Strong, Alanna; Wojcik, Monica H.; Bryant, Allison S.; Gold, Nina B. Journal: American journal of medical genetics Issue: Volume 188:Issue 4(2022) Page Start: 1118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genotype–phenotype correlation at codon 1740 of SETD2. Issue 9 (24th July 2020) Authors: Rabin, Rachel; Radmanesh, Alireza; Glass, Ian A.; Dobyns, William B.; Aldinger, Kimberly A.; Shieh, Joseph T.; Romoser, Shelby; Bombei, Hannah; Dowsett, Leah; Trapane, Pamela; Bernat, John A.; Baker, Janice; Mendelsohn, Nancy J.; Popp, Bernt; Siekmeyer, Manuela; Sorge, Ina; Sansbury, Francis Hugh... Journal: American journal of medical genetics Issue: Volume 182:Issue 9(2020) Page Start: 2037 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Global university rankings and strategic planning: a case study of Australian institutional performance. Issue 4 (3rd July 2020) Authors: Dowsett, Leah Journal: Journal of higher education policy and management Issue: Volume 42:Issue 4(2020) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Nonlethal presentations of CYP26B1‐related skeletal anomalies and multiple synostoses syndrome. Issue 9 (23rd June 2021) Authors: Grand, Katheryn; Skraban, Cara M.; Cohen, Jennifer L.; Dowsett, Leah; Mazzola, Sarah; Tarpinian, Jennifer; Bedoukian, Emma; Nesbitt, Addie; Denenberg, Beth; Lulis, Lauren; Santani, Avni; Zackai, Elaine H.; Deardorff, Matthew A. Other Names: Burkardt Deepika D'Cunha guestEditor.; Sanchez‐Lara Pedro A guestEditor.; Girisha Katta M guestEditor.; Carey John C guestEditor. Journal: American journal of medical genetics Issue: Volume 185:Issue 9(2021) Page Start: 2766 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy. Issue 8 (17th June 2019) Authors: Carter, Lauren B.; Battaglia, Agatino; Cherry, Athena; Manning, Melanie A.; Ruzhnikov, Maura RZ; Bird, Lynne M.; Dowsett, Leah; Graham, John M.; Alkuraya, Fowzan S.; Hashem, Mais; Dinulos, Mary Beth; Vallee, Stephanie; Adam, Margaret P.; Glass, Ian; Beck, Anita E.; Stevens, Cathy A.; Zackai, Elai... Journal: American journal of medical genetics Issue: Volume 179:Issue 8(2019) Page Start: 1543 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Rubinstein–Taybi syndrome in diverse populations. Issue 12 (27th September 2020) Authors: Tekendo‐Ngongang, Cedrik; Owosela, Babajide; Fleischer, Nicole; Addissie, Yonit A.; Malonga, Bryan; Badoe, Ebenezer; Gupta, Neerja; Moresco, Angélica; Huckstadt, Victoria; Ashaat, Engy A.; Hussen, Dalia Farouk; Luk, Ho‐Ming; Lo, Ivan F. M.; Hon‐Yin Chung, Brian; Fung, Jasmine L. F.; Moretti‐Ferre... Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 2939 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗