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

Year Number of Results
1980 1
1987 2
1988 3
1989 5
1990 4
1991 2
1993 1
1994 2
1995 1
1999 1
2000 2
2002 2
2004 1
2011 1
2012 1
2013 1
2014 2
2015 1
2023 0

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31 results

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Page 1
Paediatric narcolepsy: complexities of diagnosis.
Hood BM, Harbord MG. Hood BM, et al. Among authors: harbord mg. J Paediatr Child Health. 2002 Dec;38(6):618-21. doi: 10.1046/j.1440-1754.2002.00073.x. J Paediatr Child Health. 2002. PMID: 12410881 Review.
Infant-onset progressive myoclonus epilepsy.
Harbord MG, Hwang PA, Robinson BH, Becker LE, Hunjan A, Murphy EG. Harbord MG, et al. J Child Neurol. 1991 Apr;6(2):134-42. doi: 10.1177/088307389100600207. J Child Neurol. 1991. PMID: 1904460
Children's understanding of cystic fibrosis.
Harbord MG, Cross DG, Botica F, Martin AJ. Harbord MG, et al. Aust Paediatr J. 1987 Aug;23(4):241-4. doi: 10.1111/j.1440-1754.1987.tb00258.x. Aust Paediatr J. 1987. PMID: 3426458
Moebius' syndrome with unilateral cerebellar hypoplasia.
Harbord MG, Finn JP, Hall-Craggs MA, Brett EM, Baraitser M. Harbord MG, et al. J Med Genet. 1989 Sep;26(9):579-82. doi: 10.1136/jmg.26.9.579. J Med Genet. 1989. PMID: 2810343 Free PMC article.
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.
Kumar R, Corbett MA, Smith NJ, Jolly LA, Tan C, Keating DJ, Duffield MD, Utsumi T, Moriya K, Smith KR, Hoischen A, Abbott K, Harbord MG, Compton AG, Woenig JA, Arts P, Kwint M, Wieskamp N, Gijsen S, Veltman JA, Bahlo M, Gleeson JG, Haan E, Gecz J. Kumar R, et al. Among authors: harbord mg. Hum Mol Genet. 2015 Apr 1;24(7):2000-10. doi: 10.1093/hmg/ddu614. Epub 2014 Dec 11. Hum Mol Genet. 2015. PMID: 25504045
Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
Nicholl J, Waters W, Suwalski S, Brown S, Hull Y, Harbord MG, Entwistle J, Thompson S, Clark D, Pridmore C, Haan E, Barnett C, McGregor L, Liebelt J, Thompson EM, Friend K, Bain SM, Yu S, Mulley JC. Nicholl J, et al. Among authors: harbord mg. Am J Med Genet B Neuropsychiatr Genet. 2013 Jan;162B(1):24-35. doi: 10.1002/ajmg.b.32114. Epub 2012 Nov 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23184456
Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
Nicholl J, Waters W, Mulley JC, Suwalski S, Brown S, Hull Y, Barnett C, Haan E, Thompson EM, Liebelt J, Mcgregor L, Harbord MG, Entwistle J, Munt C, White D, Chitti A, Baulderstone D, Ketteridge D; Array Referral Consortium; Friend K, Bain SM, Yu S. Nicholl J, et al. Among authors: harbord mg. Pathology. 2014 Jan;46(1):41-5. doi: 10.1097/PAT.0000000000000043. Pathology. 2014. PMID: 24300712
Central nervous system malformations in Mohr's syndrome.
Reardon W, Harbord MG, Hall-Craggs MA, Kendall B, Brett EM, Baraitser M. Reardon W, et al. Among authors: harbord mg. J Med Genet. 1989 Oct;26(10):659-63. doi: 10.1136/jmg.26.10.659. J Med Genet. 1989. PMID: 2555513 Free PMC article.
31 results