1. Identification and association of recurrent ALOXE3 mutation with non‐bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families. (18th July 2018) Authors: Rahman, Simeen Ber; Mir, Asif; Ahmad, Nafees; Haider, Syed Husnain; Malik, Salman Akbar; Nasir, Muhammad Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Developmental mutant mouse models for external genitalia formation. (16th December 2018) Authors: Hashimoto, Daiki; Hyuga, Taiju; Acebedo, Alvin R.; Alcantara, Mellissa C.; Suzuki, Kentaro; Yamada, Gen Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 74 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia. (6th July 2018) Authors: Al‐Zahrani, Hams S.; Al‐Tala, Saeed; Mohamoud, Hussein S. A.; Al‐Shehri, Bandar A.; Al‐Fadhel, Saeed; Al‐Qurashi, Ali; Al‐Bishri, Ahmad; Al‐Aama, Jumana Y.; Kang, Changsoo; Betz, Regina C.; Jelani, Musharraf Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Congenital eye anomalies: More mosaic than thought?. (21st August 2018) Authors: Ohuchi, Hideyo; Sato, Keita; Habuta, Munenori; Fujita, Hirofumi; Bando, Tetsuya Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Issue Information. (26th April 2019) Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Announcement. (26th April 2019) Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 104 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular mechanisms underlying the models of neurodevelopmental disorders in maternal immune activation relevant to the placenta. (17th January 2019) Authors: Tsukada, Tsuyoshi; Shimada, Hiroki; Sakata‐Haga, Hiromi; Iizuka, Hideaki; Hatta, Toshihisa Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Potentially effective method for fetal gender determination by noninvasive prenatal testing for X‐linked disease. (6th July 2018) Authors: Noda, Yoshiteru; Kato, Takema; Kato, Asuka; Nishizawa, Haruki; Miyazaki, Jun; Ito, Mayuko; Terasawa, Sumire; Sekiya, Takao; Fujii, Takuma; Kurahashi, Hiroki Journal: Congenital anomalies Issue: Volume 59:Number 3(2019) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Issue Information. Issue 12 (December 2016) Journal: Birth defects research Issue: Volume 106:Issue 12(2016) Page Start: 989 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Letter to the editor interpreting trends in the context of previous evidence. Issue 12 (12th October 2016) Authors: Kirby, Russell S. Journal: Birth defects research Issue: Volume 106:Issue 12(2016) Page Start: 1042 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗