A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman
Seung Kyung Lee, Min Jeong Lee, Hyo Jin Lee, Bu Kyung Kim, Young Bae Sohn, Yoon-Sok Chung
J Bone Metab. 2013;20(1):57-60.   Published online 2013 May 13     DOI: https://doi.org/10.11005/jbm.2013.20.1.57
Citations to this article as recorded by Crossref logo
Aortic Arch Laterality in Chromosome 22q11.2 Deletion Syndrome: Male-Female Difference
William N. Evans, Ruben J. Acherman, Humberto Restrepo
Clinical Pediatrics.2023; 62(4): 345.     CrossRef
Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
G. E. Runova, A. V. Oderiy, I. V. Glinkina, Yu. P. Sych, S. E. Moshenina, V. V. Fadeev
Sechenov Medical Journal.2021; 12(3): 68.     CrossRef
Therapeutic monoclonal antibodies approved by FDA in 2017
Henry Hongrong Cai
MOJ Immunology.2018;[Epub]     CrossRef
Fishing for Digeorge Syndrome in A 40-YEAR-OLD Man
Christopher J. Hupfeld, Nai-Wen Chi, Kenneth Vaux
AACE Clinical Case Reports.2018; 4(2): 94.     CrossRef
Hypoparathyroidism concomitant with macrothrombocytopenia in an elderly woman with 22q11.2 deletion syndrome
Hsiu-Chien Yang, Shih-Hua Lin, Yi-Ying Wu, Chih-Chien Sung
Platelets.2018; 29(7): 733.     CrossRef
Zespół mikrodelecji 22q11.2 (zespół DiGeorge’a) bez współistniejącej wady serca – analiza fenotypu pacjentów i problemy diagnostyczne
Robert Śmigiel, Agnieszka Stembalska, Magdalena Cabała, Małgorzata Piotrowicz, Izabela Łaczmańska, Lucjusz Jakubowski, Maria Małgorzata Sąsiadek
Pediatria Polska.2015; 90(3): 181.     CrossRef
Bone status in genetic syndromes: A review
Stefano Stagi, Chiara Iurato, Elisabetta Lapi, Loredana Cavalli, Maria Luisa Brandi, Maurizio de Martino
Hormones.2015; 14(1): 19.     CrossRef