Bénichou B - Search Results

1

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H. Trochu JN, et al. Among authors: benichou b. J Am Coll Cardiol. 2000 Jun;35(7):1890-7. doi: 10.1016/s0735-1097(00)00617-3. J Am Coll Cardiol. 2000. PMID: 10841240 Free article.

2

Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

Kyndt F, Schott JJ, Trochu JN, Baranger F, Herbert O, Scott V, Fressinaud E, David A, Moisan JP, Bouhour JB, Le Marec H, Bénichou B. Kyndt F, et al. Among authors: benichou b. Am J Hum Genet. 1998 Mar;62(3):627-32. doi: 10.1086/301747. Am J Hum Genet. 1998. PMID: 9497244 Free PMC article.

3

Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosis.

Bénichou OD, Bénichou B, Copin H, De Vernejoul MC, Van Hul W. Bénichou OD, et al. Among authors: benichou b. J Bone Miner Res. 2000 Oct;15(10):1900-4. doi: 10.1359/jbmr.2000.15.10.1900. J Bone Miner Res. 2000. PMID: 11028441 Free article.

4

Possible misdiagnosis of factor VIII gene inversion in a case of severe hemophilia A.

Bénichou B, Herbert O, Huet S, André MT, Bézieau S, Le Roux MG, Fiks-Siguad M, Moisan JP. Bénichou B, et al. Blood. 1996 Apr 15;87(8):3525-6. Blood. 1996. PMID: 8605378 Free article. No abstract available.

5

Study on possible increase in twinning rate at a small village in south Brazil.

Matte U, Le Roux MG, Bénichou B, Moisan JP, Giugliani R. Matte U, et al. Among authors: benichou b. Acta Genet Med Gemellol (Roma). 1996;45(4):431-7. doi: 10.1017/s0001566000000829. Acta Genet Med Gemellol (Roma). 1996. PMID: 9181177

6

Rapid diagnostic test for detection of Cys282Tyr mutation in hereditary hemochromatosis.

Andre MT, Jacquemont S, Renault S, Airaud F, Herbert O, Moisan JP, Benichou B, Raguenes O. Andre MT, et al. Among authors: benichou b. Dig Dis Sci. 1998 Jun;43(6):1339-40. doi: 10.1023/a:1018884530378. Dig Dis Sci. 1998. PMID: 9635628 No abstract available.

7

[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies].

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboulet S, Benichou B, Zeviani M, Le Paslier D, et al. Melki J, et al. Among authors: benichou b. C R Seances Soc Biol Fil. 1994;188(5-6):495-8. C R Seances Soc Biol Fil. 1994. PMID: 7780792 Review. French.

8

Osteopetrosis as a model for studying bone resorption.

Bénichou OD, Bénichou B, de Vernejoul MC. Bénichou OD, et al. Among authors: benichou b. Rev Rhum Engl Ed. 1998 Dec;65(12):778-87. Rev Rhum Engl Ed. 1998. PMID: 9923047 Review. No abstract available.

9

Identification and characterization of a spinal muscular atrophy-determining gene.

Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, et al. Lefebvre S, et al. Among authors: benichou b. Cell. 1995 Jan 13;80(1):155-65. doi: 10.1016/0092-8674(95)90460-3. Cell. 1995. PMID: 7813012 Free article.

10

De novo and inherited deletions of the 5q13 region in spinal muscular atrophies.

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboullet S, Bénichou B, Zeviani M, Le Paslier D, et al. Melki J, et al. Among authors: benichou b. Science. 1994 Jun 3;264(5164):1474-7. doi: 10.1126/science.7910982. Science. 1994. PMID: 7910982

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