Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Syndrome and BMPR1B[original query] |
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| The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. Journal of medical genetics 2004 Jul 41 (7): 484-91. Howe J R, Sayed M G, Ahmed A F, Ringold J, Larsen-Haidle J, Merg A, Mitros F A, Vaccaro C A, Petersen G M, Giardiello F M, Tinley S T, Aaltonen L A, Lynch H |
| Rare copy number variants identified in prune belly syndrome. European journal of medical genetics 2017 11 61 (3): 145-151. Boghossian Nansi S, Sicko Robert J, Giannakou Andreas, Dimopoulos Aggeliki, Caggana Michele, Tsai Michael Y, Yeung Edwina H, Pankratz Nathan, Cole Benjamin R, Romitti Paul A, Browne Marilyn L, Fan Ruzong, Liu Aiyi, Kay Denise M, Mills James |
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
PLoS medicine 2020 06 17 (6): e1003132. Dapas Matthew, Lin Frederick T J, Nadkarni Girish N, Sisk Ryan, Legro Richard S, Urbanek Margrit, Hayes M Geoffrey, Dunaif Andr |
| A genotype-first analysis in a cohort of Mullerian anomaly. Journal of human genetics 2022 1 67 (6): 347-352. Tian Weijie, Chen Na, Ye Yang, Ma Congcong, Qin Chenglu, Niu Yuchen, Xiaoxin L, Zhao Lina, Zhao Hengqiang, Liang Ze, Song Shuang, Wang Yuan, Chen Zefu, Lin Jiachen, Yan Zihui, Duan Jiali, Zhao Sen, Zhang Terry Jianguo, Qiu Guixing, Wu Zhihong, Wu Nan, Zhu L |
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