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227 results
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Haplotype XV of the Y-chromosome is the main haplotype in West-Europe.
Diéterlen F, Lucotte G. Diéterlen F, et al. Among authors: lucotte g. Biomed Pharmacother. 2005 Jun;59(5):269-72. doi: 10.1016/j.biopha.2004.08.023. Biomed Pharmacother. 2005. PMID: 15890489
Absence of a close linkage between Alzheimer's disease susceptibility gene and a polymorphic DNA probe coding for beta-amyloid.
David F, Lucotte G. David F, et al. Among authors: lucotte g. Biomed Pharmacother. 1988;42(9):575-7. Biomed Pharmacother. 1988. PMID: 2907297
Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in families.
Mercier G, Burckel A, Bathelier C, Boillat E, Lucotte G. Mercier G, et al. Among authors: lucotte g. Genet Couns. 1998;9(3):181-6. Genet Couns. 1998. PMID: 9777338
Linkage analysis of French families with facioscapulohumeral muscular dystrophy.
Lucotte G, Berriche S, Fardeau M. Lucotte G, et al. J Med Genet. 1989 Aug;26(8):485-6. doi: 10.1136/jmg.26.8.485. J Med Genet. 1989. PMID: 2769721 Free PMC article.
A new TaqI polymorphism detected by the cDNA encoding amyloid beta protein of Alzheimer's disease.
David F, Robakis NK, Lucotte G. David F, et al. Among authors: lucotte g. Nucleic Acids Res. 1987 Nov 11;15(21):9103. doi: 10.1093/nar/15.21.9103. Nucleic Acids Res. 1987. PMID: 2891111 Free PMC article. No abstract available.
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Among authors: lucotte g. Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192. Am J Hum Genet. 1999. PMID: 9915947 Free PMC article.
Y chromosome DNA polymorphisms in two African populations.
Lucotte G, Guérin P, Hallé L, Loirat F, Hazout S. Lucotte G, et al. Am J Hum Genet. 1989 Jul;45(1):16-20. Am J Hum Genet. 1989. PMID: 2568089 Free PMC article.
G542X as a probable Phoenician cystic fibrosis mutation.
Loirat F, Hazout S, Lucotte G. Loirat F, et al. Among authors: lucotte g. Hum Biol. 1997 Jun;69(3):419-25. Hum Biol. 1997. PMID: 9164051
Pattern of gradient of apolipoprotein E allele *4 frequencies in western Europe.
Lucotte G, Loirat F, Hazout S. Lucotte G, et al. Hum Biol. 1997 Apr;69(2):253-62. Hum Biol. 1997. PMID: 9057348
Complete map of cystic fibrosis mutation DF508 frequencies in Western Europe and correlation between mutation frequencies and incidence of disease.
Lucotte G, Hazout S, De Braekeleer M. Lucotte G, et al. Hum Biol. 1995 Oct;67(5):797-803. Hum Biol. 1995. PMID: 8543293
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