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

Year Number of Results
1984 1
1985 8
1986 11
1987 13
1988 4
1989 5
1990 2
1991 6
1992 7
1993 13
1994 5
1995 7
1996 9
1997 9
1998 15
1999 8
2000 7
2001 7
2002 8
2003 8
2004 3
2005 14
2006 3
2007 5
2008 3
2009 7
2010 9
2011 11
2012 12
2013 18
2014 10
2015 15
2016 6
2017 4
2018 8
2019 4
2020 1
2021 3
2022 2
2023 3
2024 0

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279 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.
Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Grozeva D, Carss K, Spasic-Boskovic O, Tejada MI, Gecz J, Shaw M, Corbett M, Haan E, Thompson E, Friend K, Hussain Z, Hackett A, Field M, Renieri A, Stevenson R, Schwartz C, Floyd JA, Bentham J, Cosgrove C, Keavney B, Bhattacharya S; Italian X-linked Mental Retardation Project; UK10K Consortium; GOLD Consortium; Hurles M, Raymond FL. Grozeva D, et al. Hum Mutat. 2015 Dec;36(12):1197-204. doi: 10.1002/humu.22901. Epub 2015 Sep 30. Hum Mutat. 2015. PMID: 26350204 Free PMC article.
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.
The cystic fibrosis locus.
Williamson R, Wainwright B, Cooper C, Scambler P, Farrall M, Estivill X, Pedersen P. Williamson R, et al. Among authors: scambler p. Enzyme. 1987;38(1-4):8-13. doi: 10.1159/000469185. Enzyme. 1987. PMID: 3326737 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.
The Renal Gene Ontology Annotation Initiative.
Alam-Faruque Y, Dimmer EC, Huntley RP, O'Donovan C, Scambler P, Apweiler R. Alam-Faruque Y, et al. Among authors: scambler p. Organogenesis. 2010 Apr-Jun;6(2):71-5. doi: 10.4161/org.6.2.11294. Organogenesis. 2010. PMID: 20885853 Free PMC article. Review.
279 results