11. Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome. (27th October 2019) Authors: Senthilraja, Manickavasagam; Chapla, Aaron; Jebasingh, Felix K.; Naik, Dukhabhandhu; Paul, Thomas V.; Thomas, Nihal Other Names: Suri Mohnish Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Two Novel Variants in the ATRX Gene Associated with Variable Phenotypes. (6th November 2019) Authors: Hettiarachchi, D.; Pathirana, B. A. P. S.; Kumarasiri, P. J.; Dissanayake, V. H. W. Other Names: Cotter Philip D. Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Case of Inherited Partial AZFa Deletion without Impact on Male Fertility. (31st October 2019) Authors: Alksere, Baiba; Berzina, Dace; Dudorova, Alesja; Conka, Una; Andersone, Santa; Pimane, Evija; Krasucka, Sandra; Blumberga, Arita; Dzalbs, Aigars; Grinfelde, Ieva; Vedmedovska, Natalija; Fodina, Violeta; Erenpreiss, Juris Other Names: Suri Mohnish Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. The Relationship between Polymorphisms in the Vitamin D Receptor Gene and Bone Mineral Density in Postmenopausal Women. (9th January 2014) Authors: Moran, Jose M.; Rodriguez-Velasco, Francisco J.; Roncero-Martin, Raul; Rey-Sanchez, Purificación; Martinez, Mariana; Pedrera-Zamorano, Juan D. Other Names: Fasching P. A. Academic Editor.; Nacak M. Academic Editor. Journal: ISRN genetics Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Polyadenylation in Plants : Methods and Protocols /: Methods and Protocols. (2015) Editors: Hunt, Arthur G; Li, Qingshun Quinn Record Type: Book Extent: 1 online resource, illustrations View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Genetics, evolution and radiation : crossing borders, the interdisciplinary legacy of Nikolay W. Timofeeff-Ressovsky /: crossing borders, the interdisciplinary legacy of Nikolay W. Timofeeff-Ressovsky. ([2016]) Editors: Korogodina, V. L; Mothersill, C (Carmel); Inge-Vechtomov, S. G; Seymour, C Record Type: Book Extent: 1 online resource, illustrations View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. (28th December 2019) Authors: Petter, Cristian; Moreira, Lilia Maria Azevedo; Riegel, Mariluce Other Names: Paracchini Silvia Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case. (22nd December 2019) Authors: Sabir, A. H.; Ryan, G.; Mohammed, Z.; Kirk, J.; Kiely, N.; Thyagarajan, M.; Cole, T. Other Names: Yapijakis Christos Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Corrigendum to "Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features". (24th November 2019) Authors: Riley, Jacquelyn D.; Stefaniuk, Catherine M.; Erenberg, Francine; Erwin, Angelika L.; Palange, Lauren; Astbury, Caroline Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome. (28th December 2019) Authors: Morgan, T. M.; Colazo, J. M.; Duncan, L.; Hamid, R.; Joos, K. M. Other Names: Ban Yoshiyuki Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗