Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 5 (of 5 Records) |
Query Trace: Macroglossia[original query] |
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Prevalence of tongue lesions among Turkish schoolchildren. Saudi medical journal 2005 12 26 (12): 1962-7. Ugar-Cankal Dilek, Denizci Senem, Hocaoglu Turg |
Obstructive Sleep Apnea in Children With Beckwith-Wiedemann Syndrome. Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine 2019 3 15 (3): 375-381. Cielo Christopher M, Duffy Kelly A, Taylor Jesse A, Marcus Carole L, Kalish Jennifer |
Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric Study. The Journal of clinical pediatric dentistry 2020 11 44 (4): 262-267. Gürsoy Semra, Hazan Filiz, Kaderli Bülent, Me?e Timur, Tükün Ajl |
Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants. Cancers 2022 8 14 (15): . Cardoso Leila Cabral de Almeida, Parra Alejandro, Gil Cristina Ríos, Arias Pedro, Gallego Natalia, Romanelli Valeria, Kantaputra Piranit Nik, Lima Leonardo, Llerena Júnior Juan Clinton, Arberas Claudia, Guillén-Navarro Encarna, Nevado Julián, Spanish OverGrowth Registry Initiative , Tenorio-Castano Jair, Lapunzina Pab |
Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome. Annals of laboratory medicine 2022 Nov 42 (6): 668-677. Kim Hwa Young, Shin Choong Ho, Lee Young Ah, Shin Chang Ho, Kim Gu-Hwan, Ko Jung M |
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