1. Analysis of cardiac anomalies in VACTERL association. Issue 12 (December 2013) Authors: Cunningham, Bridget K.; Hadley, Donald W.; Hannoush, Hwaida; Meltzer, Andrew C.; Niforatos, Nickie; Pineda‐Alvarez, Daniel; Sachdev, Vandana; Warren‐Mora, Nicole; Solomon, Benjamin D. Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 792 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder‐exstrophy‐epispadias complex. Issue 12 (2nd August 2013) Authors: Qi, Lihong; Wang, Mei; Yagnik, Garima; Mattheisen, Manuel; Gearhart, John P.; lakshmanan, Yegappan; Ebert, Anne‐Karolin; Rösch, Wolfgang; Ludwig, Michael; Draaken, Markus; Reutter, Heiko; Boyadjiev, Simeon A. Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 759 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic Basis of Congenital Upper Limb Anomalies: Analysis of 487 Cases of a Specialized Clinic. Issue 12 (December 2013) Authors: Carli, Diana; Fairplay, Tracy; Ferrari, Paola; Sartini, Silvana; Lando, Mario; Garagnani, Lorenzo; Di Gennaro, Giovanni Luigi; Di Pancrazio, Luciana; Bianconi, Giorgia; Elmakky, Amira; Bernasconi, Sergio; Landi, Antonio; Percesepe, Antonio Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 798 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mandibulofacial dysostosis (Treacher‐Collins syndrome) in the fetus: Novel association with pectus carinatum in a molecularly confirmed case and review of the fetal phenotype. Issue 12 (29th November 2013) Authors: Konstantinidou, Anastasia E.; Tassoulas, Iason; Kallipolitis, Georgios; Gasparatos, Spyros; Velissariou, Voula; Paraskevakou, Helen Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 774 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel mutations in ADAMTSL2 gene underlying geleophysic dysplasia in families from United Arab Emirates. Issue 12 (6th September 2013) Authors: Ben‐Salem, Salma; Hertecant, Jozef; Al‐Shamsi, Aisha M.; Ali, Bassam R.; Al‐Gazali, Lihadh Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 764 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Patient with disorganization syndrome: Surgical procedures, Pathology, and potential causes. Issue 12 (4th December 2013) Authors: Vallejo, Oscar Girón; Benítez Sánchez, María del Carmen; Cánovas, Cesar Salcedo; Ontiveros, Joanna Díez; Ruiz Jiménez, José Ignacio; Bermejo‐Sánchez, Eva; Martínez‐Frías, María Luisa Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 781 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Prenatal diagnosis of femoral–facial syndrome: Report of two cases. Issue 12 (19th November 2013) Authors: Silvas, Emil; Rypens, Françoise; Jovanovic, Mubina; Delezoide, Anne‐Lise; Patey, Natalie Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 770 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prenatal ultrasound findings observed in the Wolf‐hirschhorn syndrome: Data from the registry of congenital malformations in auvergne. Issue 12 (6th November 2013) Authors: Debost‐Legrand, Anne; Goumy, Carole; Laurichesse‐Delmas, Hélène; Déchelotte, Pierre; Beaufrère, Anne‐Marie; Lémery, Didier; Francannet, Christine; Gallot, Denis Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 806 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Second study on the recurrence risk of isolated esophageal atresia with or without trachea‐esophageal fistula among first‐degree relatives: No evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum. Issue 12 (5th December 2013) Authors: Choinitzki, Vera; Zwink, Nadine; Bartels, Enrika; Baudisch, Friederike; Boemers, Thomas M.; Hölscher, Alice; Turial, Salmai; Bachour, Haitham; Heydweiller, Andreas; Kurz, Ralf; Bartmann, Peter; Pauly, Markus; Brokmeier, Ulrike; Leutner, Andreas; Nöthen, Markus M.; Schumacher, Johannes; Jenetzky, ... Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 786 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cord. Issue 12 (12th November 2013) Authors: Liu, Jinglan; Jethva, Reena; Del, Michael T.; Hauptman, John E.; Pascasio, Judy M.; de Chadarévian, Jean‐Pierre Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 812 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗