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

Year Number of Results
1953 1
1955 1
1957 2
1958 1
1959 1
1961 1
1963 1
1964 2
1969 1
1971 1
1972 1
1975 1
2014 2
2015 1
2017 1
2018 2
2020 1
2024 0

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19 results

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Page 1
Color blindness.
Raymond LF. Raymond LF. Ann Allergy. 1971 Apr;29(4):214-6. Ann Allergy. 1971. PMID: 5317317 No abstract available.
A clinical and molecular characterisation of CRB1-associated maculopathy.
Khan KN, Robson A, Mahroo OAR, Arno G, Inglehearn CF, Armengol M, Waseem N, Holder GE, Carss KJ, Raymond LF, Webster AR, Moore AT, McKibbin M, van Genderen MM, Poulter JA, Michaelides M; UK Inherited Retinal Disease Consortium. Khan KN, et al. Among authors: raymond lf. Eur J Hum Genet. 2018 May;26(5):687-694. doi: 10.1038/s41431-017-0082-2. Epub 2018 Feb 1. Eur J Hum Genet. 2018. PMID: 29391521 Free PMC article.
Biallelic mutations of TBC1D24 in exercise-induced paroxysmal dystonia.
Steel D, Heim J, Kruer MC, Sanchis-Juan A, Raymond LF, Eunson P, Kurian MA. Steel D, et al. Among authors: raymond lf. Mov Disord. 2020 Feb;35(2):372-373. doi: 10.1002/mds.27981. Epub 2020 Jan 10. Mov Disord. 2020. PMID: 31922275 No abstract available.
Managing clinically significant findings in research: the UK10K example.
Kaye J, Hurles M, Griffin H, Grewal J, Bobrow M, Timpson N, Smee C, Bolton P, Durbin R, Dyke S, Fitzpatrick D, Kennedy K, Kent A, Muddyman D, Muntoni F, Raymond LF, Semple R, Spector T; UK 10K. Kaye J, et al. Among authors: raymond lf. Eur J Hum Genet. 2014 Sep;22(9):1100-4. doi: 10.1038/ejhg.2013.290. Epub 2014 Jan 15. Eur J Hum Genet. 2014. PMID: 24424120 Free PMC article.
Assessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases.
Ellingford JM, Horn B, Campbell C, Arno G, Barton S, Tate C, Bhaskar S, Sergouniotis PI, Taylor RL, Carss KJ, Raymond LFL, Michaelides M, Ramsden SC, Webster AR, Black GCM. Ellingford JM, et al. Among authors: raymond lfl. J Med Genet. 2018 Feb;55(2):114-121. doi: 10.1136/jmedgenet-2017-104791. Epub 2017 Oct 26. J Med Genet. 2018. PMID: 29074561 Free PMC article.
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
Chaudhry A, Noor A, Degagne B, Baker K, Bok LA, Brady AF, Chitayat D, Chung BH, Cytrynbaum C, Dyment D, Filges I, Helm B, Hutchison HT, Jeng LJ, Laumonnier F, Marshall CR, Menzel M, Parkash S, Parker MJ; DDD Study; Raymond LF, Rideout AL, Roberts W, Rupps R, Schanze I, Schrander-Stumpel CT, Speevak MD, Stavropoulos DJ, Stevens SJ, Thomas ER, Toutain A, Vergano S, Weksberg R, Scherer SW, Vincent JB, Carter MT. Chaudhry A, et al. Among authors: raymond lf. Clin Genet. 2015 Sep;88(3):224-33. doi: 10.1111/cge.12482. Epub 2014 Oct 14. Clin Genet. 2015. PMID: 25131214
Dental factors in migraine: report of a case.
RAYMOND LF, MONICA WS. RAYMOND LF, et al. Ann Otol Rhinol Laryngol. 1958 Mar;67(1):145-7. doi: 10.1177/000348945806700111. Ann Otol Rhinol Laryngol. 1958. PMID: 13521630 No abstract available.
Staphylococcus sensitivity in chorioretinitis.
RAYMOND LF. RAYMOND LF. Am J Ophthalmol. 1959 Dec;48:846-7. doi: 10.1016/0002-9394(59)90634-8. Am J Ophthalmol. 1959. PMID: 14436632 No abstract available.
ALLERGY AND CHRONIC SIMPLE GLAUCOMA.
RAYMOND LF. RAYMOND LF. Ann Allergy. 1964 Mar;22:146-50. Ann Allergy. 1964. PMID: 14130389 No abstract available.
19 results