Lucotte G - Search Results

1

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Sarfarazi M, Upadhyaya M, Padberg G, Pericak-Vance M, Siddique T, Lucotte G, Lunt P. Sarfarazi M, et al. Among authors: lucotte g. J Med Genet. 1989 Aug;26(8):481-4. doi: 10.1136/jmg.26.8.481. J Med Genet. 1989. PMID: 2769720 Free PMC article.

2

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.

3

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease.

Andrew S, Theilmann J, Almqvist E, Norremolle A, Lucotte G, Anvret M, Sorensen SA, Turpin JC, Hayden MR. Andrew S, et al. Among authors: lucotte g. Clin Genet. 1993 Jun;43(6):286-94. doi: 10.1111/j.1399-0004.1993.tb03820.x. Clin Genet. 1993. PMID: 8370147

4

Mapping of probe p49f to the proximal part of the human Y chromosome long arm.

Quack B, Guérin P, Ruffié J, Lucotte G. Quack B, et al. Among authors: lucotte g. Cytogenet Cell Genet. 1988;47(4):232. doi: 10.1159/000132557. Cytogenet Cell Genet. 1988. PMID: 3416658

5

Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity.

Gal A, Wirth B, Kääriäinen H, Lucotte G, Landais P, Gillessen-Kaesbach G, Müller-Wiefel DE, Zerres K. Gal A, et al. Among authors: lucotte g. Clin Genet. 1989 Jan;35(1):13-9. doi: 10.1111/j.1399-0004.1989.tb02900.x. Clin Genet. 1989. PMID: 2924430

6

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.

Telenius H, Kremer HP, Theilmann J, Andrew SE, Almqvist E, Anvret M, Greenberg C, Greenberg J, Lucotte G, Squitieri F, et al. Telenius H, et al. Among authors: lucotte g. Hum Mol Genet. 1993 Oct;2(10):1535-40. doi: 10.1093/hmg/2.10.1535. Hum Mol Genet. 1993. PMID: 8268906

7

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.

8

A DNA probe detecting multiple haplotypes of the human Y chromosome.

Ngo KY, Vergnaud G, Johnsson C, Lucotte G, Weissenbach J. Ngo KY, et al. Among authors: lucotte g. Am J Hum Genet. 1986 Apr;38(4):407-18. Am J Hum Genet. 1986. PMID: 3010708 Free PMC article.

9

Allele doses of apolipoprotein E type epsilon 4 in sporadic late-onset Alzheimer's disease.

Lucotte G, Aouizérate A, Gérard N, Turpin JC, Landais P. Lucotte G, et al. Am J Med Genet. 1995 Dec 18;60(6):566-9. doi: 10.1002/ajmg.1320600617. Am J Med Genet. 1995. PMID: 8825898

10

A new TaqI BO variant detected with the p49 probe on the human Y chromosome.

Guérin P, Rouger P, Lucotte G. Guérin P, et al. Among authors: lucotte g. Nucleic Acids Res. 1988 Aug 11;16(15):7759. doi: 10.1093/nar/16.15.7759. Nucleic Acids Res. 1988. PMID: 2901073 Free PMC article.

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