Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: PNPT1[original query] |
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The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature. BMC medical genetics 2010 11 (1): 96. Zhao Jianhua, Li Mingyao, Bradfield Jonathan P, Zhang Haitao, Mentch Frank D, Wang Kai, Sleiman Patrick M, Kim Cecilia E, Glessner Joseph T, Hou Cuiping, Keating Brendan J, Thomas Kelly A, Garris Maria L, Deliard Sandra, Frackelton Edward C, Otieno F George, Chiavacci Rosetta M, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population. Journal of advanced research 2021 7 31 13-24. Souissi Amal, Ben Said Mariem, Ben Ayed Ikhlas, Elloumi Ines, Bouzid Amal, Mosrati Mohamed Ali, Hasnaoui Mehdi, Belcadhi Malek, Idriss Nabil, Kamoun Hassen, Gharbi Nourhene, Gibriel Abdullah A, Tlili Abdelaziz, Masmoudi Sab |
Genome-wide association study identifies five risk loci for pernicious anemia. Nature communications 2021 6 12 (1): 3761. Laisk Triin, Lepamets Maarja, Koel Mariann, Abner Erik, , Mägi Reed |
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India. Annals of human genetics 2021 Aug . Vanniya S Paridhy, Chandru Jayasankaran, Jeffrey Justin Margret, Rabinowitz Tom, Brownstein Zippora, Krishnamoorthy Mathuravalli, Avraham Karen B, Cheng Le, Shomron Noam, Srisailapathy C R Srikuma |
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