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

Year Number of Results
1971 1
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1975 1
1979 2
1984 2
1985 4
1986 3
1987 6
1988 1
1989 4
1990 3
1991 4
1992 1
1993 1
1995 3
1996 3
1997 5
2000 1
2001 1
2003 3
2005 2
2006 1
2007 1
2008 1
2010 1
2011 5
2012 4
2013 6
2014 4
2015 2
2016 1
2017 1
2018 5
2019 1
2021 1
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2024 1

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86 results

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Page 1
Mitotic recombinatory evolution in acute leukemia.
Papenhausen P, Kelly CA, Zhang Z, Penton A. Papenhausen P, et al. Cancer Genet. 2023 Jun;274-275:33-40. doi: 10.1016/j.cancergen.2023.02.003. Epub 2023 Mar 11. Cancer Genet. 2023. PMID: 36966725
Cleft palate and complex chromosome rearrangements.
Kousseff BG, Papenhausen P, Neu RL, Essig YP, Saraceno CA. Kousseff BG, et al. Among authors: papenhausen p. Clin Genet. 1992 Sep;42(3):135-42. doi: 10.1111/j.1399-0004.1992.tb03225.x. Clin Genet. 1992. PMID: 1327590 Review.
Intraventricular twin fetuses in fetu.
Huddle LN, Fuller C, Powell T, Hiemenga JA, Yan J, Deuell B, Lyders EM, Bodurtha JN, Papenhausen PR, Jackson-Cook CK, Pandya A, Jaworski M, Tye GW, Ritter AM. Huddle LN, et al. Among authors: papenhausen pr. J Neurosurg Pediatr. 2012 Jan;9(1):17-23. doi: 10.3171/2011.10.PEDS11196. J Neurosurg Pediatr. 2012. PMID: 22208315
Phenotypes Associated with SHOX Deficiency.
Ross JL, Scott C Jr, Marttila P, Kowal K, Nass A, Papenhausen P, Abboudi J, Osterman L, Kushner H, Carter P, Ezaki M, Elder F, Wei F, Chen H, Zinn AR. Ross JL, et al. Among authors: papenhausen p. J Clin Endocrinol Metab. 2001 Dec;86(12):5674-80. doi: 10.1210/jcem.86.12.8125. J Clin Endocrinol Metab. 2001. PMID: 11739418
86 results