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

Year Number of Results
1985 6
1986 6
1987 8
1988 4
1989 2
1990 2
1991 4
1992 6
1993 9
1994 3
1995 3
1996 4
1997 6
1998 7
1999 3
2000 4
2001 4
2002 7
2003 7
2004 2
2005 9
2006 3
2007 2
2008 2
2009 5
2010 5
2011 7
2012 8
2013 15
2014 4
2015 9
2016 4
2017 2
2018 8
2019 2
2020 1
2021 2
2022 1
2023 2
2024 0

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177 results

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Page 1
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Among authors: scambler pj. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
Molecular genetics of 22q11.2 deletion syndrome.
Morrow BE, McDonald-McGinn DM, Emanuel BS, Vermeesch JR, Scambler PJ. Morrow BE, et al. Among authors: scambler pj. Am J Med Genet A. 2018 Oct;176(10):2070-2081. doi: 10.1002/ajmg.a.40504. Am J Med Genet A. 2018. PMID: 30380194 Free PMC article. Review.
Mechanisms and cell lineages in lymphatic vascular development.
Jafree DJ, Long DA, Scambler PJ, Ruhrberg C. Jafree DJ, et al. Among authors: scambler pj. Angiogenesis. 2021 May;24(2):271-288. doi: 10.1007/s10456-021-09784-8. Epub 2021 Apr 6. Angiogenesis. 2021. PMID: 33825109 Free PMC article. Review.
Clinical and molecular effects of CHD7 in the heart.
Corsten-Janssen N, Scambler PJ. Corsten-Janssen N, et al. Among authors: scambler pj. Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):487-495. doi: 10.1002/ajmg.c.31590. Epub 2017 Oct 31. Am J Med Genet C Semin Med Genet. 2017. PMID: 29088513 Review.
Human HOX gene mutations.
Goodman FR, Scambler PJ. Goodman FR, et al. Among authors: scambler pj. Clin Genet. 2001 Jan;59(1):1-11. doi: 10.1034/j.1399-0004.2001.590101.x. Clin Genet. 2001. PMID: 11206481 Review.
The cystic fibrosis gene.
Scambler PJ. Scambler PJ. Arch Dis Child. 1989 Dec;64(12):1647-8. doi: 10.1136/adc.64.12.1647. Arch Dis Child. 1989. PMID: 2696430 Free PMC article. Review. No abstract available.
Evolving concepts in human renal dysplasia.
Woolf AS, Price KL, Scambler PJ, Winyard PJ. Woolf AS, et al. Among authors: scambler pj. J Am Soc Nephrol. 2004 Apr;15(4):998-1007. doi: 10.1097/01.asn.0000113778.06598.6f. J Am Soc Nephrol. 2004. PMID: 15034102 Review.
Velo-cardio-facial syndrome: a review of 120 patients.
Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ. Goldberg R, et al. Among authors: scambler pj. Am J Med Genet. 1993 Feb 1;45(3):313-9. doi: 10.1002/ajmg.1320450307. Am J Med Genet. 1993. PMID: 8434617 Review.
The 22q11 deletion syndromes.
Scambler PJ. Scambler PJ. Hum Mol Genet. 2000 Oct;9(16):2421-6. doi: 10.1093/hmg/9.16.2421. Hum Mol Genet. 2000. PMID: 11005797 Review.
177 results