Bahuau M - Search Results

1

Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness.

Bahuau M, Vidaud D, Kujas M, Palangié A, Assouline B, Chaignaud-Lebreton M, Prieur M, Vidaud M, Harpey JP, Lafourcade J, Caille B. Bahuau M, et al. Ann Genet. 1997;40(2):78-91. Ann Genet. 1997. PMID: 9259954

2

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

Bahuau M, Vidaud D, Jenkins RB, Bièche I, Kimmel DW, Assouline B, Smith JS, Alderete B, Cayuela JM, Harpey JP, Caille B, Vidaud M. Bahuau M, et al. Cancer Res. 1998 Jun 1;58(11):2298-303. Cancer Res. 1998. PMID: 9622062

3

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome.

Bahuau M, Houdayer C, Assouline B, Blanchet-Bardon C, Le Merrer M, Lyonnet S, Giraud S, Récan D, Lakhdar H, Vidaud M, Vidaud D. Bahuau M, et al. Am J Med Genet. 1998 Jan 23;75(3):265-72. Am J Med Genet. 1998. PMID: 9475595

4

TaqMan PCR-based gene dosage assay for predictive testing in individuals from a cancer family with INK4 locus haploinsufficiency.

Laurendeau I, Bahuau M, Vodovar N, Larramendy C, Olivi M, Bieche I, Vidaud M, Vidaud D. Laurendeau I, et al. Among authors: bahuau m. Clin Chem. 1999 Jul;45(7):982-6. Clin Chem. 1999. PMID: 10388473

5

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.

Bahuau M, Flintoff W, Assouline B, Lyonnet S, Le Merrer M, Prieur M, Guilloud-Bataille M, Feingold N, Munnich A, Vidaud M, Vidaud D. Bahuau M, et al. Am J Med Genet. 1996 Dec 18;66(3):347-55. doi: 10.1002/(SICI)1096-8628(19961218)66:3<347::AID-AJMG20>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8985499

6

Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B).

Bahuau M, Laurendeau I, Pelet A, Assouline B, Lamireau T, Taine L, Le Bail B, Vergnes P, Gallet S, Vidaud M, Lyonnet S, Lacombe D, Vidaud D. Bahuau M, et al. J Med Genet. 2000 Feb;37(2):146-50. doi: 10.1136/jmg.37.2.146. J Med Genet. 2000. PMID: 10712107 Free PMC article. No abstract available.

7

Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.

Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M. Houdayer C, et al. Among authors: bahuau m. Ann Genet. 1999;42(2):69-74. Ann Genet. 1999. PMID: 10434119

8

GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotype.

Bahuau M, Pelet A, Vidaud D, Lamireau T, LeBail B, Munnich A, Vidaud M, Lyonnet S, Lacombe D. Bahuau M, et al. J Med Genet. 2001 Sep;38(9):638-43. doi: 10.1136/jmg.38.9.638. J Med Genet. 2001. PMID: 11565554 Free PMC article. No abstract available.

9

Orofacial cleft defects: inference from nature and nurture.

Houdayer C, Bahuau M. Houdayer C, et al. Among authors: bahuau m. Ann Genet. 1998;41(2):89-117. Ann Genet. 1998. PMID: 9706339 Review.

10

Genetics of nonsyndromic cleft lip with or without cleft palate: is there a Mendelian sub-entity?

Gajdos V, Bahuau M, Robert-Gnansia E, Francannet C, Cordier S, Bonaïti-Pellié C. Gajdos V, et al. Among authors: bahuau m. Ann Genet. 2004 Jan-Mar;47(1):29-39. doi: 10.1016/j.anngen.2003.12.002. Ann Genet. 2004. PMID: 15050872

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