Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
Go Hun Seo (Seo GH), Ja Hye Kim (Kim JH), Ja Hyang Cho (Cho JH), Gu-Hwan Kim (Kim GH), Eul-Ju Seo (Seo EJ), Beom Hee Lee (Lee BH), Jin-Ho Choi (Choi JH), Han-Wook Yoo (Yoo HW)
Clin Exp Pediatr. 2016;59(1):16-23.   Published online 2016 Jan 22     DOI: https://doi.org/10.3345/kjp.2016.59.1.16
Citations to this article as recorded by Crossref logo
Outcome of Vertical Expandable Prosthetic Titanium Rib (VEPTR) Instrumentation in Scoliosis Associated With 1p36 Deletion Syndrome: A Case Report
Ozair Bin Majid, Mohammed A Al Rushud, Zayed Al-Zayed, Ghadeer Alsager, Jehangir A Bhat
Cureus.2022;[Epub]     CrossRef
Monosomy 1p36: Report of a cohort of 13 Asian Indian patients
Neerja Gupta, Ravneet Kaur, Shubha Phadke, Pankaj Sharma, Sheela Nampoothiri, Deepti Saxena, Madhulika Kabra
American Journal of Medical Genetics Part A.2022; 188(4): 1317.     CrossRef
Comprehensive Assessment of Fetal Bilateral Ventriculomegaly Based on Genetic Disorders, Cytomegalovirus Infection, Extra Prenatal Imaging and Pregnancy Outcomes in a Tertiary Referral Center
Danhua Guo, Deqin He, Qingmei Shen, Na Lin, Shuqiong He, Yifang Dai, Ying Li, Liangpu Xu, Xiaoqing Wu
International Journal of General Medicine.2021; Volume 14: 7719.     CrossRef
Farklı prezentasyon gösteren iki vaka; 1p 36 delesyon sendromu
Hilal AYDIN, İbrahim Hakan BUCAK, Mehmet GEYİK, Haydar BAĞIŞ
Adıyaman Üniversitesi Sağlık Bilimleri Dergisi.2020; 6(1): 128.     CrossRef
Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation
Dalia F. Hussen, Alaa K. Kamel, Mona K. Mekkawy, Engy A. Ashaat, Mona O. El Ruby
Molecular Syndromology.2020; 11(5-6): 284.     CrossRef
Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome
Masatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, Maki Ogawa, Fumihiko Suzuki, Takema Kato, Shunsuke Miyai, Rie Kawamura, Hidehito Inagaki, Hiroki Kurahashi, Jun Murotsuki
Case Reports in Obstetrics and Gynecology.2019; 2019: 1.     CrossRef
Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review
M. Greco, P. Ferrara, G. Farello, P. Striano, A. Verrotti
Epilepsy Research.2018; 139: 92.     CrossRef
Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications
Alberto Verrotti, Marco Greco, Gaia Varriale, Agnese Tamborino, Salvatore Savasta, Marco Carotenuto, Maurizio Elia, Francesca Operto, Lucia Margari, Vincenzo Belcastro, Angelo Selicorni, Elena Freri, Sara Matricardi, Tiziana Granata, Francesca Ragona, Giu
Acta Neurologica Scandinavica.2018; 138(6): 523.     CrossRef