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Midori Awazu

Showing results (51-60 of 54) with videos related to

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Hypertension Research : Official Journal of the Japanese Society of Hypertension|January 28, 2021
Association of childhood anthropometric measurements and laboratory parameters with high blood pressure in young adultsTatsuhiko Azegami, Keiko Uchida, Fujiyo Arima, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and cleftingToshiki Takenouchi, Hironobu Okuno, Rika Kosaki, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 2004
The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemiaFusako Komoda, Takashi Sekine, Jun Inatomi, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)Megumi Yoshimura-Furuhata, Akira Nishimura-Tadaki, Yoshiro Amano, et al.
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Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|January 28, 2021
Association of childhood anthropometric measurements and laboratory parameters with high blood pressure in young adultsTatsuhiko Azegami, Keiko Uchida, Fujiyo Arima, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and cleftingToshiki Takenouchi, Hironobu Okuno, Rika Kosaki, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 2004
The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemiaFusako Komoda, Takashi Sekine, Jun Inatomi, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)Megumi Yoshimura-Furuhata, Akira Nishimura-Tadaki, Yoshiro Amano, et al.
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