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Results by year

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

Year Number of Results
1950 3
1951 5
1952 1
1953 7
1954 8
1955 3
1956 1
1957 2
1958 4
1959 1
1960 1
1961 1
1963 2
1964 1
1966 1
1967 2
1968 4
1969 1
1970 1
1971 1
1973 1
1974 1
1975 1
1976 3
1977 1
1979 4
1980 4
1981 1
1982 6
1983 3
1984 4
1985 2
1986 1
1988 1
1990 2
1991 2
1992 1
1993 2
1996 6
1997 1
1998 1
2000 4
2001 4
2002 5
2003 5
2004 2
2005 1
2006 4
2007 5
2008 4
2009 6
2010 5
2011 6
2012 6
2013 9
2014 7
2015 6
2016 12
2017 14
2018 13
2019 8
2020 8
2021 15
2022 13
2023 10
2024 2

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242 results

Results by year

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Page 1
45,X/46,XY mosaicism: Clinical manifestations and long term follow-up.
Alkhunaizi E, Albrecht JP, Aarabi M, Witchel SF, Wherrett D, Babul-Hirji R, Dupuis A, Chiniara L, Chater-Diehl E, Shago M, Shuman C, Rajkovic A, Yatsenko SA, Chitayat D. Alkhunaizi E, et al. Among authors: shuman c. Am J Med Genet A. 2024 Mar;194(3):e63451. doi: 10.1002/ajmg.a.63451. Epub 2023 Oct 26. Am J Med Genet A. 2024. PMID: 37882230
Beckwith-Wiedemann Syndrome.
Shuman C, Kalish JM, Weksberg R. Shuman C, et al. 2000 Mar 3 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Mar 3 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301568 Free Books & Documents. Review.
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition.
Bogatan S, Shugar A, Wasim S, Ball S, Schmidt C, Chitayat D, Shuman C, Cytrynbaum C. Bogatan S, et al. Among authors: shuman c. PEC Innov. 2022 Dec 6;2:100115. doi: 10.1016/j.pecinn.2022.100115. eCollection 2023 Dec. PEC Innov. 2022. PMID: 37214507 Free PMC article.
Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Luca S, Clausen M, Shaw A, Lee W, Krishnapillai S, Adi-Wauran E, Faghfoury H, Costain G, Jobling R, Aronson M, Liston E, Silver J, Shuman C, Chad L, Hayeems RZ, Bombard Y; Genetics Navigator Study Team. Luca S, et al. Among authors: shuman c. Hum Genet. 2023 Mar;142(3):321-330. doi: 10.1007/s00439-022-02512-2. Epub 2023 Jan 11. Hum Genet. 2023. PMID: 36629921 Free PMC article.
242 results