Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Shock and SERPINH1[original query] |
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A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans. Proceedings of the National Academy of Sciences of the United States of America 2006 Sep 103 (36): 13463-7. Wang Hongyan, Parry Samuel, Macones George, Sammel Mary D, Kuivaniemi Helena, Tromp Gerard, Argyropoulos George, Halder Indrani, Shriver Mark D, Romero Roberto, Strauss Jerome |
Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2018 3 29 (6): 1389-1396. Song Y, Zhao D, Xu X, Lv F, Li L, Jiang Y, Wang O, Xia W, Xing X, Li |
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