1. 8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features. Issue 4 (October 2020) Authors: LaBranche, Jennifer T.N.; Argiropoulos, Bob; Thomas, Mary Ann Journal: Clinical dysmorphology Issue: Volume 29:Issue 4(2020:Oct.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition. Issue 4 (5th January 2016) Authors: Crone, Megan; Thomas, Mary Ann Journal: American journal of medical genetics Issue: Volume 170:Issue 4(2016) Page Start: 1095 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism. Issue 4 (26th July 2021) Authors: Phillips, Eliza A.; Caluseriu, Oana; Schlade-Bartusiak, Kamilla; Chernos, Judy; McLeod, D. Ross; Thomas, Mary Ann Journal: Clinical dysmorphology Issue: Volume 30:Issue 4(2021) Page Start: 173 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism. Issue 4 (October 2021) Authors: Phillips, Eliza A.; Caluseriu, Oana; Schlade-Bartusiak, Kamilla; Chernos, Judy; McLeod, D. Ross; Thomas, Mary Ann Journal: Clinical dysmorphology Issue: Volume 30:Issue 4(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families. Issue 12 (7th October 2020) Authors: Chang, Caitlin A.; Di Donato, Nataliya; Hackmann, Karl; Argiropoulos, Bob; Ferreira, Patrick; Innes, A. Micheil; Thomas, Mary Ann Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 3040 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism. Issue 8 (27th May 2020) Authors: Woodward, Kristine E.; Shah, Ravi M.; Benseler, Susanne; Wei, Xing‐Chang; Ng, Denise; Grossman, Jennifer; Hahn, Christopher; Thomas, Mary Ann; Wright, Nicola A. M.; Appendino, Juan Pablo Journal: Pediatric blood & cancer Issue: Volume 67:Issue 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency. Issue 6 (August 2021) Authors: Martin, Georgina; Thomas, Mary Ann; Wei, Xing-Chang; Le, Doan Journal: Journal of pediatric hematology/oncology Issue: Volume 43:Issue 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Effects of Brief Depression and Anxiety Management Training on a US Army Division's Primary Care Providers. Issue 5 (28th January 2020) Authors: Amin, Rohul; Thomas, Mary Ann Journal: Military medicine Issue: Volume 185:Issue 5/6(2020) Page Start: e719 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Issue 4 (13th January 2021) Authors: Zarate, Yuri A.; Bosanko, Katherine A.; Thomas, Mary Ann; Miller, David T.; Cusmano‐Ozog, Kristina; Martinez‐Monseny, Antonio; Curry, Cynthia J.; Graham, John M.; Velsher, Lea; Bekheirnia, Mir Reza; Seidel, Veronica; Dedousis, Demitrios; Mitchell, Anna L.; DiMarino, Amy M.; Riess, Angelika; Balas... Journal: Clinical genetics Issue: Volume 99:Issue 4(2021) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. MG-128 Use of prenatal array comparative genomic hybridization in cases of fetal structural cardiac anomalies: New cases and review of the literature. (4th December 2015) Authors: Lazier, Joanna; Thomas, Mary Ann Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 1 Page Start: A7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗