![]() |
A Leri-Weill dyschondrosteosis patient confirmed by mutation analysis of
Won Bok Choi, Seung Hyeon Seo, Woo Hyun Yoo, Su Young Kim, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2015;20(3):162-165. Published online 2015 Sep 30 DOI: https://doi.org/10.6065/apem.2015.20.3.162
|
Citations to this article as recorded by
Clinical and Genetic Characteristics of 23 Korean Patients with
Haploinsufficiency of the Short-stature Homeobox-containing Gene
Jeong-Seon Lee, Hwa Young Kim, Young-Ah Lee, Seong-Young Lee, Tae-Joon Cho, Jung Min Ko
Experimental and Clinical Endocrinology & Diabetes.2021; 129(08): 611. CrossRef Leri-Weill dyschondrosteosis in a newborn presenting with respiratory failure due to severe micrognathia
Mi Hyeon Gang, Jianne Lee, Yong Wook Lee, Ji Hye Shin, Han Hyuk Lim, Yoo-Mi Kim, Mea-young Chang
Journal of Genetic Medicine.2020; 17(2): 108. CrossRef Heterozygous Deletion in Exons 4-5 of SHOX Gene in a Patient Diagnosed as Idiopathic Short Stature
Anna David, Imre Zoltán Kun, Gábor Nyírő, Zsuzsánna Szántó, Attila Patócs
Acta Medica Marisiensis.2017; 63(3): 155. CrossRef
|