Boutrand L - Search Results

1

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.

Attié T, Till M, Pelet A, Amiel J, Edery P, Boutrand L, Munnich A, Lyonnet S. Attié T, et al. Among authors: boutrand l. Hum Mol Genet. 1995 Dec;4(12):2407-9. doi: 10.1093/hmg/4.12.2407. Hum Mol Genet. 1995. PMID: 8634719 No abstract available.

2

Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.

Attié T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand L, Beldjord C, Nihoul-Fékété C, Munnich A, et al. Attié T, et al. Among authors: boutrand l. Hum Mol Genet. 1995 Aug;4(8):1381-6. doi: 10.1093/hmg/4.8.1381. Hum Mol Genet. 1995. PMID: 7581377

3

BRCA2 mutations in hereditary breast and ovarian cancer in France.

Serova-Sinilnikova OM, Boutrand L, Stoppa-Lyonnet D, Bressac-de-Paillerets B, Dubois V, Lasset C, Janin N, Bignon YJ, Longy M, Maugard C, Lidereau R, Leroux D, Frebourg T, Mazoyer S, Lenoir GM. Serova-Sinilnikova OM, et al. Among authors: boutrand l. Am J Hum Genet. 1997 May;60(5):1236-9. Am J Hum Genet. 1997. PMID: 9150172 Free PMC article. No abstract available.

4

Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies.

Vandenberghe N, Upadhyaya M, Gatignol A, Boutrand L, Boucherat M, Chazot G, Vandenberghe A, Latour P. Vandenberghe N, et al. Among authors: boutrand l. J Med Genet. 2002 Dec;39(12):e81. doi: 10.1136/jmg.39.12.e81. J Med Genet. 2002. PMID: 12471219 Free PMC article. No abstract available.

5

Germline brca2 sequence variants in patients with ocular melanoma.

Sinilnikova OM, Egan KM, Quinn JL, Boutrand L, Lenoir GM, Stoppa-Lyonnet D, Desjardins L, Levy C, Goldgar D, Gragoudas ES. Sinilnikova OM, et al. Among authors: boutrand l. Int J Cancer. 1999 Jul 30;82(3):325-8. doi: 10.1002/(sici)1097-0215(19990730)82:3<325::aid-ijc3>3.0.co;2-g. Int J Cancer. 1999. PMID: 10399947 Free article. Clinical Trial.

6

Alternative exon 3 splicing of the human major protein zero gene in white blood cells and peripheral nerve tissue.

Besançon R, Prost AL, Konecny L, Latour P, Petiot P, Boutrand L, Kopp N, Mularoni A, Chamba G, Vandenberghe A. Besançon R, et al. Among authors: boutrand l. FEBS Lett. 1999 Sep 3;457(3):339-42. doi: 10.1016/s0014-5793(99)01069-8. FEBS Lett. 1999. PMID: 10471804 Free article.

7

Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplication.

Latour P, Boutrand L, Levy N, Bernard R, Boyer A, Claustrat F, Chazot G, Boucherat M, Vandenberghe A. Latour P, et al. Among authors: boutrand l. Clin Chem. 2001 May;47(5):829-37. Clin Chem. 2001. PMID: 11325885

8

Variations in primer sequences are the origin of allele drop-out at loci D13S317 and CD4.

Boutrand L, Egyed B, Füredi S, Mommers N, Mertens G, Vandenberghe A. Boutrand L, et al. Int J Legal Med. 2001;114(4-5):295-7. doi: 10.1007/s004140000183. Int J Legal Med. 2001. PMID: 11355416

9

Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090.

Mertens G, Mommers N, Boutrand L, Gielis M, Vandenberghe A. Mertens G, et al. Among authors: boutrand l. Int J Legal Med. 2001 Aug;115(1):40-4. doi: 10.1007/s004140100227. Int J Legal Med. 2001. PMID: 11599767

10

Analysis of eight STR loci in two Hungarian populations.

Egyed B, Füredi S, Angyal M, Boutrand L, Vandenberghe A, Woller J, Pádár Z. Egyed B, et al. Among authors: boutrand l. Forensic Sci Int. 2000 Sep 11;113(1-3):25-7. doi: 10.1016/s0379-0738(00)00191-2. Forensic Sci Int. 2000. PMID: 10978596

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