1. Can we identify WHIM in infancy? Opportunities with the public newborn screening process. Issue 2 (9th October 2022) Authors: Yilmaz, Melis; Potts, David Evan; Geier, Christoph; Walter, Jolan E. Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 215 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cover Image, Volume 190, Number 2, June 2022. Issue 2 (18th October 2022) Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnostic experiences of Duchenne families and their preferences for newborn screening: A mixed‐methods study. Issue 2 (9th August 2022) Authors: Crossnohere, Norah L.; Armstrong, Niki; Fischer, Ryan; Bridges, John F. P. Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 169 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dispatches from Biotech beginning BeginNGS: Rapid newborn genome sequencing to end the diagnostic and therapeutic odyssey. Issue 2 (11th October 2022) Authors: Kingsmore, Stephen F. Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 243 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Duchenne expert physician perspectives on Duchenne newborn screening and early Duchenne care. Issue 2 (5th August 2022) Authors: Armstrong, Niki; Schrader, Rachel; Fischer, Ryan; Crossnohere, Norah Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 162 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Georgia state spinal muscular atrophy newborn screening experience: Screening assay performance and early clinical outcomes. Issue 2 (26th September 2022) Authors: Elkins, Kathryn; Wittenauer, Angela; Hagar, Arthur F.; Logan, Rachel; Sekul, Elizabeth; Xiang, Yijin; Verma, Sumit; Wilcox, William R. Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Newborn screening and the recommended uniform screening panel: Optimal submissions and suggested improvements based on an advocacy organization's decade‐long experience. Issue 2 (22nd September 2022) Authors: Ellinwood, N. Matthew Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Newborn screening for Duchenne muscular dystrophy‐early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy. Issue 2 (24th September 2022) Authors: Gruber, Dorota; Lloyd‐Puryear, Michele; Armstrong, Niki; Scavina, Mena; Tavakoli, Norma P.; Brower, Amy M.; Caggana, Michele; Chung, Wendy K. Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Newborn screening for Fabry disease in Oregon: Approaching the iceberg of A143T and variants of uncertain significance. Issue 2 (26th September 2022) Authors: Viall, Sarah; Dennis, Anna; Yang, Amy Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 206 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Newborn screening for neurodevelopmental diseases: Are we there yet?. Issue 2 (15th July 2022) Authors: Chung, Wendy K.; Berg, Jonathan S.; Botkin, Jeffrey R.; Brenner, Steven E.; Brosco, Jeffrey P.; Brothers, Kyle B.; Currier, Robert J.; Gaviglio, Amy; Kowtoniuk, Walter E.; Olson, Colleen; Lloyd‐Puryear, Michele; Saarinen, Annamarie; Sahin, Mustafa; Shen, Yufeng; Sherr, Elliott H.; Watson, Michael... Other Names: Brower Amy guestEditor.; Chan Kee guestEditor. Journal: American journal of medical genetics Issue: Volume 190:Issue 2(2022) Page Start: 222 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗