Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Syringomyelia[original query] |
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[The analysis of the SpI (1546G>T) polymorphism of the Col1A1 gene and the FokI (3663T>C) polymorphism of the vitamin D receptor gene in patients with syringomyelia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2007 107 (9): 60-6. Abulgatina A S, Khusainova R I, Khidiiatova I M, Kutuev I A, Mirsaev T R, Borisova N A, Khusnutdinova E |
Frequency and characteristics of congenital intraspinal abnormalities in a cohort of 128 patients with congenital scoliosis. Journal of craniovertebral junction & spine 2020 2 10 (4): 229-233. Mariscal Gonzalo, Nuñez Jorge H, Bhatia Sanjay, Marsh Robert, Barrios Carlos, Domenech-Fernández Ped |
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