Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and SEMA3D[original query] |
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| Effects of SEMA3 polymorphisms in Hirschsprung disease patients. Pediatric surgery international 2016 Nov 32 (11): 1025-1028. Gunadi , Makhmudi Akhmad, Agustriani Nunik, Rochad |
Genome-wide association study identifies new loci for albuminuria in the Japanese population.
Clinical and experimental nephrology 2020 Apr . Okuda Hiroshi, Okamoto Koji, Abe Michiaki, Ishizawa Kota, Makino Satoshi, Tanabe Osamu, Sugawara Junichi, Hozawa Atsushi, Tanno Kozo, Sasaki Makoto, Tamiya Gen, Yamamoto Masayuki, Ito Sadayoshi, Ishii Tadas |
| Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients. Frontiers in pediatrics 2020 3 8 60. Gunadi , Kalim Alvin Santoso, Budi Nova Yuli Prasetyo, Hafiq Hamzah Muhammad, Maharani Annisa, Febrianti Maharani, Ryantono Fiko, Yulianda Dicky, Iskandar Kristy, Veltman Joris |
| Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease. Ear and hearing 2020 11 41 (6): 1598-1605. Roman-Naranjo Pablo, Gallego-Martinez Alvaro, Soto-Varela Andrés, Aran Ismael, Moleon Maria Del Carmen, Espinosa-Sanchez Juan Manuel, Amor-Dorado Juan Carlos, Batuecas-Caletrio Angel, Perez-Vazquez Paz, Lopez-Escamez Jose Anton |
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