1. A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy. Issue 11 (21st September 2017) Authors: Vatti, Lohith; Fitzgerald‐Butt, Sara M.; McBride, Kim L. Journal: American journal of medical genetics Issue: Volume 173:Issue 11(2017) Page Start: 2995 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy. Issue 11 (21st September 2017) Authors: Vatti, Lohith; Fitzgerald‐Butt, Sara M.; McBride, Kim L. Journal: American journal of medical genetics Issue: Volume 173:Issue 11(2017) Page Start: 2995 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America. Issue 2 (12th October 2022) Authors: Rickman, Allison F.; Fitzgerald‐Butt, Sara M.; Spoonamore, Katherine G.; Ware, Stephanie M.; Helm, Benjamin M. Journal: Journal of genetic counseling Issue: Volume 32:Issue 2(2023) Page Start: 362 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Assessing genetic counselors' graduate school education and training in congenital heart defects. Issue 3 (7th December 2021) Authors: Ahmad, Aaliya; Fitzgerald‐Butt, Sara M.; Ware, Stephanie M.; Ison, Hannah E.; Elmore, Lindsey R.; Helm, Benjamin M. Journal: Journal of genetic counseling Issue: Volume 31:Issue 3(2022) Page Start: 735 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease. Issue 4 (10th March 2017) Authors: Morales, Ana; Allain, Dawn C.; Arscott, Patricia; James, Emily; MacCarrick, Gretchen; Murray, Brittney; Tichnell, Crystal; Shikany, Amy R.; Spencer, Sara; Fitzgerald‐Butt, Sara M.; Kushner, Jessica D.; Munn, Christi; Smith, Emily; Spoonamore, Katherine G.; Tandri, Harikrishna S.; Kay, W. Aaron Journal: Journal of genetic counseling Issue: Volume 26:Issue 4(2017) Page Start: 669 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease. Issue 4 (4th May 2017) Authors: Morales, Ana; Allain, Dawn C.; Arscott, Patricia; James, Emily; MacCarrick, Gretchen; Murray, Brittney; Tichnell, Crystal; Shikany, Amy R.; Spencer, Sara; Fitzgerald‐Butt, Sara M.; Kushner, Jessica D.; Munn, Christi; Smith, Emily; Spoonamore, Katherine G.; Tandri, Harikrishna S.; Aaron Kay, W. Journal: Journal of genetic counseling Issue: Volume 26:Issue 4(2017) Page Start: 689 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic knowledge and attitudes of parents of children with congenital heart defects. Issue 12 (24th September 2014) Authors: Fitzgerald‐Butt, Sara M.; Klima, Jennifer; Kelleher, Kelly; Chisolm, Deena; McBride, Kim L. Journal: American journal of medical genetics Issue: Volume 164:Issue 12(2014.) Page Start: 3069 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study. Issue 2 (27th September 2021) Authors: Richardson, Brooke; Fitzgerald‐Butt, Sara M.; Spoonamore, Katherine G.; Wetherill, Leah; Helm, Benjamin M.; Breman, Amy M. Journal: Journal of genetic counseling Issue: Volume 31:Issue 2(2022) Page Start: 479 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain. (16th April 2015) Authors: Huang, Wenrui; Liang, Jingsheng; Yuan, Chen‐Ching; Kazmierczak, Katarzyna; Zhou, Zhiqun; Morales, Ana; McBride, Kim L.; Fitzgerald‐Butt, Sara M.; Hershberger, Ray E.; Szczesna‐Cordary, Danuta Journal: FEBS journal Issue: Volume 282:Number 12(2015) Page Start: 2379 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗