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

Year Number of Results
1932 1
1945 1
1946 11
1947 5
1948 1
1949 1
1950 2
1951 4
1952 5
1953 1
1954 2
1955 1
1956 2
1957 3
1958 1
1959 2
1960 1
1962 3
1963 9
1964 3
1965 3
1966 3
1967 1
1968 4
1969 2
1970 1
1972 2
1974 1
1975 1
1976 3
1978 1
1979 2
1980 2
1981 2
1982 2
1983 9
1984 10
1985 10
1986 9
1987 17
1988 13
1989 13
1990 7
1991 19
1992 6
1993 8
1994 9
1995 6
1996 7
1997 3
1998 3
1999 5
2000 4
2001 8
2002 4
2003 4
2004 6
2005 9
2006 7
2007 3
2008 6
2009 5
2010 5
2011 7
2012 9
2013 5
2014 3
2015 4
2016 3
2017 4
2018 7
2019 2
2020 3
2021 3
2022 5
2023 3
2024 4

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358 results

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Page 1
Notes from the Field: A Cluster of Multi-Strain Invasive Pneumococcal Disease Among Persons Experiencing Homelessness and Use of Pneumococcal Conjugate Vaccine - El Paso County, Colorado, 2022.
Callaway J, Durbin K, Zachary H, Barnes MM, Kobayashi M, Chochua S, Gayou N, Albanese B. Callaway J, et al. MMWR Morb Mortal Wkly Rep. 2023 Nov 17;72(46):1277-1278. doi: 10.15585/mmwr.mm7246a5. MMWR Morb Mortal Wkly Rep. 2023. PMID: 37971930 Free PMC article. No abstract available.
Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory records.
Loong L, Huntley C, McRonald F, Santaniello F, Pethick J, Torr B, Allen S, Tulloch O, Goel S, Shand B, Rahman T, Luchtenborg M, Garrett A, Barber R, Bedenham T, Bourn D, Bradshaw K, Brooks C, Bruty J, Burghel GJ, Butler S, Buxton C, Callaway A, Callaway J, Drummond J, Durkie M, Field J, Jenkins L, McVeigh TP, Mountford R, Nyanhete R, Petrides E, Robinson R, Scott T, Stinton V, Tellez J, Wallace AJ, Yarram-Smith L, Sahan K, Hallowell N, Eccles DM, Pharoah P, Tischkowitz M, Antoniou AC, Evans DG, Lalloo F, Norbury G, Morris E, Burn J, Hardy S, Turnbull C. Loong L, et al. Among authors: callaway j. J Med Genet. 2023 Jul;60(7):669-678. doi: 10.1136/jmg-2022-108800. Epub 2022 Dec 26. J Med Genet. 2023. PMID: 36572524 Free PMC article.
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B).
Lin S, Sanchez-Bretaño A, Leslie JS, Williams KB, Lee H, Thomas NS, Callaway J, Deline J, Ratnayaka JA, Baralle D, Schmitt MA, Norman CS, Hammond S, Harlalka GV, Ennis S, Cross HE, Wenger O, Crosby AH, Baple EL, Self JE. Lin S, et al. Among authors: callaway j. NPJ Genom Med. 2022 Jan 13;7(1):2. doi: 10.1038/s41525-021-00275-9. NPJ Genom Med. 2022. PMID: 35027574 Free PMC article.
358 results