31. 58th Annual Teratology Society Meeting. Issue 9 (15th May 2018) Journal: Birth defects research Issue: Volume 110:Issue 9(2018) Page Start: 667 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
32. 59th Annual Teratology Society Meeting. Issue 9 (13th May 2019) Journal: Birth defects research Issue: Volume 111:Issue 9(2019) Page Start: 405 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
33. 5‐Aminolevulinic acid can ameliorate language dysfunction of patients with ATR‐X syndrome. (16th January 2020) Authors: Wada, Takahito; Suzuki, Shuichi; Shioda, Norifumi Journal: Congenital anomalies Issue: Volume 60:Number 5(2020) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
34. 5‐year experience of a tertiary center in major congenital abnormalities in singleton pregnancies. Issue 8 (11th January 2020) Authors: Beksac, M. Sinan; Fadiloglu, Erdem; Unal, Canan; Cetiner, Sibel; Tanacan, Atakan Journal: Birth defects research Issue: Volume 112:Issue 8(2020) Page Start: 633 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
35. 60th Anniversary comments. Issue 12 (19th July 2020) Authors: Hoberman, Alan M. Other Names: Holmes Lewis B. guestEditor. Journal: Birth defects research Issue: Volume 112:Issue 12(2020) Page Start: 942 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
36. 6p21.33 Deletion encompassing CSNK2B is associated with relative macrocephaly, facial dysmorphism, and mild intellectual disability. Issue 3 (19th March 2021) Authors: Ohashi, Ikuko; Kuroda, Yukiko; Enomoto, Yumi; Murakami, Hiroaki; Masuno, Mitsuo; Kurosawa, Kenji Journal: Clinical dysmorphology Issue: Volume 30:Issue 3(2021) Page Start: 139 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
37. 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) ↗
38. A 10-Month-Old Infant Presenting With Signs of Precocious Puberty Secondary to a Sclerosing Stromal Tumor of the Ovary in the Absence of Hormonal Elevation. (July 2019) Authors: Squillaro, Anthony I; Zhou, Shengmei; Thomas, Stefanie M; Kim, Eugene S Journal: Pediatric and developmental pathology Issue: Volume 22:Number 4(2019) Page Start: 375 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
39. A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects. (17th May 2017) Authors: Shimojima, Keiko; Okamoto, Nobuhiko; Yamamoto, Toshiyuki Journal: Congenital anomalies Issue: Volume 58:Number 1(2018) Page Start: 36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
40. A 14-Year Old Girl with Reversible Hypoglycemic Episodes: The Role of ASVS. (January 2015) Authors: Smith, Alisha; Thornton, Paul S.; Galliani, Carlos A.; Miller, James P.; Dykes, Jennifer; Leung-Pineda, Van Journal: Pediatric and developmental pathology Issue: Volume 18:Number 1(2015) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗