Amelia Kirby to Female
This is a "connection" page, showing publications Amelia Kirby has written about Female.
Connection Strength
0.059
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Navalkele P, Guzman M, Kirby A, Pinz H, Kemp J. Familial Pediatric Clear Cell Meningioma With Germline SMARCE1 Mutation in the United States. J Neuropathol Exp Neurol. 2020 11 01; 79(11):1250-1252.
Score: 0.013
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Bajinting A, Munoz-Abraham AS, Osei H, Kirby AJ, Greenspon J, Villalona GA. To operate or not to operate? Assessing NSQIP surgical outcomes in trisomy 18 patients. J Pediatr Surg. 2021 Mar; 56(3):565-568.
Score: 0.013
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Lee JS, Becker BA, Kirby A, Knutsen AP. Chromosome 1q23.3q31.1 deletion associated with decreased newborn screening of T cell receptor rearrangement circles (TRECs). Ann Allergy Asthma Immunol. 2018 07; 121(1):125-126.
Score: 0.011
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Ratchford TL, Kirby AJ, Pinz H, Patel DR. Congenital Diarrhea From DGAT1 Mutation Leading to Electrolyte Derangements, Protein-losing Enteropathy, and Rickets. J Pediatr Gastroenterol Nutr. 2018 03; 66(3):e82-e83.
Score: 0.011
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Zarate YA, Smith-Hicks CL, Greene C, Abbott MA, Siu VM, Calhoun ARUL, Pandya A, Li C, Sellars EA, Kaylor J, Bosanko K, Kalsner L, Basinger A, Slavotinek AM, Perry H, Saenz M, Szybowska M, Wilson LC, Kumar A, Brain C, Balasubramanian M, Dubbs H, Ortiz-Gonzalez XR, Zackai E, Stein Q, Powell CM, Schrier Vergano S, Britt A, Sun A, Smith W, Bebin EM, Picker J, Kirby A, Pinz H, Bombei H, Mahida S, Cohen JS, Fatemi A, Vernon HJ, McClellan R, Fleming LR, Knyszek B, Steinraths M, Velasco Gonzalez C, Beck AE, Golden-Grant KL, Egense A, Parikh A, Raimondi C, Angle B, Allen W, Schott S, Algrabli A, Robin NH, Ray JW, Everman DB, Gambello MJ, Chung WK. Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome. . 2018 04; 176(4):925-935.
Score: 0.011