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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2009 1
2011 1
2012 1
2017 1
2018 3
2019 4
2020 4
2021 1
2022 2
2023 1
2024 0

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15 results

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Page 1
Antenatally detected liver and biliary pathology.
Shaughnessy MP, Spencer-Manzon M, Cowles RA. Shaughnessy MP, et al. Among authors: spencer manzon m. Semin Pediatr Surg. 2020 Aug;29(4):150939. doi: 10.1016/j.sempedsurg.2020.150939. Epub 2020 Jul 24. Semin Pediatr Surg. 2020. PMID: 32861443 Review.
A retrospective cohort analysis of the Yale pediatric genomics discovery program.
Al-Ali S, Jeffries L, Faustino EVS, Ji W, Mis E, Konstantino M, Zerillo C, Jiang YH, Spencer-Manzon M, Bale A, Zhang H, McGlynn J, McGrath JM, Tremblay T, Brodsky NN, Lucas CL, Pierce R, Deniz E, Khokha MK, Lakhani SA. Al-Ali S, et al. Among authors: spencer manzon m. Am J Med Genet A. 2022 Oct;188(10):2869-2878. doi: 10.1002/ajmg.a.62918. Epub 2022 Jul 28. Am J Med Genet A. 2022. PMID: 35899841 Free PMC article.
Platelet activation in cystic fibrosis.
O'Sullivan BP, Linden MD, Frelinger AL 3rd, Barnard MR, Spencer-Manzon M, Morris JE, Salem RO, Laposata M, Michelson AD. O'Sullivan BP, et al. Among authors: spencer manzon m. Blood. 2005 Jun 15;105(12):4635-41. doi: 10.1182/blood-2004-06-2098. Epub 2005 Feb 10. Blood. 2005. PMID: 15705796 Free article.
Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 Variants.
Landim-Vieira M, Johnston JR, Ji W, Mis EK, Tijerino J, Spencer-Manzon M, Jeffries L, Hall EK, Panisello-Manterola D, Khokha MK, Deniz E, Chase PB, Lakhani SA, Pinto JR. Landim-Vieira M, et al. Among authors: spencer manzon m. Front Physiol. 2020 Jan 22;10:1612. doi: 10.3389/fphys.2019.01612. eCollection 2019. Front Physiol. 2020. PMID: 32038292 Free PMC article.
Liver transplantation for glycogen storage disease type Ia.
Reddy SK, Austin SL, Spencer-Manzon M, Koeberl DD, Clary BM, Desai DM, Smith AD, Kishnani PS. Reddy SK, et al. Among authors: spencer manzon m. J Hepatol. 2009 Sep;51(3):483-90. doi: 10.1016/j.jhep.2009.05.026. Epub 2009 Jun 17. J Hepatol. 2009. PMID: 19596478
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3).
Thompson MD, Li X, Spencer-Manzon M, Andrade DM, Murakami Y, Kinoshita T, Carpenter TO. Thompson MD, et al. Among authors: spencer manzon m. Genes (Basel). 2023 Jan 30;14(2):359. doi: 10.3390/genes14020359. Genes (Basel). 2023. PMID: 36833286 Free PMC article.
15 results