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

Year Number of Results
1978 1
1988 1
1989 1
1990 1
1991 1
1992 2
1993 2
1994 1
1995 2
1997 1
1999 1
2000 1
2001 2
2002 1
2003 1
2006 1
2007 1
2008 1
2011 1
2012 2
2014 1
2015 1
2016 1
2017 1
2019 1
2021 1
2024 0

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31 results

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Page 1
Pachydermoperiostosis in childhood.
Sinha GP, Curtis P, Haigh D, Lealman GT, Dodds W, Bennett CP. Sinha GP, et al. Among authors: bennett cp. Br J Rheumatol. 1997 Nov;36(11):1224-7. doi: 10.1093/rheumatology/36.11.1224. Br J Rheumatol. 1997. PMID: 9402870
Pseudotrisomy 13 syndrome.
Seller MJ, Bennett CP. Seller MJ, et al. Among authors: bennett cp. Am J Med Genet. 1990 Oct;37(2):297. doi: 10.1002/ajmg.1320370235. Am J Med Genet. 1990. PMID: 2248307 No abstract available.
Environmental Contamination of Contact Precaution and Non-Contact Precaution Patient Rooms in Six Acute Care Facilities.
Tanner WD, Leecaster MK, Zhang Y, Stratford KM, Mayer J, Visnovsky LD, Alhmidi H, Cadnum JL, Jencson AL, Koganti S, Bennett CP, Donskey CJ, Noble-Wang J, Reddy SC, Rose LJ, Watson L, Ide E, Wipperfurth T, Safdar N, Arasim M, Macke C, Roman P, Krein SL, Loc-Carrillo C, Samore MH. Tanner WD, et al. Among authors: bennett cp. Clin Infect Dis. 2021 Jan 29;72(Suppl 1):S8-S16. doi: 10.1093/cid/ciaa1602. Clin Infect Dis. 2021. PMID: 33512527 Free PMC article.
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome.
Hollstein R, Parry DA, Nalbach L, Logan CV, Strom TM, Hartill VL, Carr IM, Korenke GC, Uppal S, Ahmed M, Wieland T, Markham AF, Bennett CP, Gillessen-Kaesbach G, Sheridan EG, Kaiser FJ, Bonthron DT. Hollstein R, et al. Among authors: bennett cp. J Med Genet. 2015 Dec;52(12):797-803. doi: 10.1136/jmedgenet-2015-103344. Epub 2015 Sep 30. J Med Genet. 2015. PMID: 26424145 Free PMC article.
Evolutionarily assembled cis-regulatory module at a human ciliopathy locus.
Lee JH, Silhavy JL, Lee JE, Al-Gazali L, Thomas S, Davis EE, Bielas SL, Hill KJ, Iannicelli M, Brancati F, Gabriel SB, Russ C, Logan CV, Sharif SM, Bennett CP, Abe M, Hildebrandt F, Diplas BH, Attié-Bitach T, Katsanis N, Rajab A, Koul R, Sztriha L, Waters ER, Ferro-Novick S, Woods CG, Johnson CA, Valente EM, Zaki MS, Gleeson JG. Lee JH, et al. Among authors: bennett cp. Science. 2012 Feb 24;335(6071):966-9. doi: 10.1126/science.1213506. Epub 2012 Jan 26. Science. 2012. PMID: 22282472 Free PMC article.
Deletion 9p and sex reversal.
Bennett CP, Docherty Z, Robb SA, Ramani P, Hawkins JR, Grant D. Bennett CP, et al. J Med Genet. 1993 Jun;30(6):518-20. doi: 10.1136/jmg.30.6.518. J Med Genet. 1993. PMID: 8326498 Free PMC article.
Duplication involving band 4q32 with minimal clinical effect.
Maltby EL, Barnes IC, Bennett CP. Maltby EL, et al. Among authors: bennett cp. Am J Med Genet. 1999 Apr 23;83(5):431. doi: 10.1002/(sici)1096-8628(19990423)83:5<431::aid-ajmg20>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10232760 No abstract available.
Trisomy 15 mosaicism in an IVF fetus.
Bennett CP, Davis T, Seller MJ. Bennett CP, et al. J Med Genet. 1992 Oct;29(10):745-6. doi: 10.1136/jmg.29.10.745. J Med Genet. 1992. PMID: 1433239 Free PMC article.
31 results