Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Abnormalities and HOXA1[original query] |
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The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death. Medical science monitor : international medical journal of experimental and clinical research 2014 20 1531-8. Lozi? Bernarda, Krželj Vjekoslav, Kuzmi?-Prusac Ivana, Kuzmani?-Šamija Radenka, ?apkun Vesna, Lasan Ružica, Zemunik Tatija |
Characteristics of genetic alterations of peripheral T-cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG). British journal of haematology 2021 7 194 (4): 718-729. Ohki Kentaro, Kiyokawa Nobutaka, Watanabe Satoru, Iwafuchi Hideto, Nakazawa Astuko, Ishiwata Keisuke, Ogata-Kawata Hiroko, Nakabayashi Kazuhiko, Okamura Kohji, Tanaka Fumiko, Fukano Reiji, Hata Kenichiro, Mori Tetsuya, Moriya Saito Akiko, Hayashi Yasuhide, Taga Takashi, Sekimizu Masahiro, Kobayashi Ryoji, |
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- Page last updated:Mar 25, 2024
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