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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Fraser Syndrome and FREM1[original query]
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Journal of the American Society of Nephrology : JASN 2014 Sep 25 (9): 1917-22.
Kohl Stefan, Hwang Daw-Yang, Dworschak Gabriel C, Hilger Alina C, Saisawat Pawaree, Vivante Asaf, Stajic Natasa, Bogdanovic Radovan, Reutter Heiko M, Kehinde Elijah O, Tasic Velibor, Hildebrandt Friedhe
Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism.
BMC urology 2017 12 17 (1): 112.
Mizuno Kentaro, Nakane Akihiro, Nishio Hidenori, Moritoki Yoshinobu, Kamisawa Hideyuki, Kurokawa Satoshi, Kato Taiki, Ando Ryosuke, Maruyama Tetsuji, Yasui Takahiro, Hayashi Yuta
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