Amati P - Search Results

1

Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.

Longy M, Coulon V, Duboué B, David A, Larrègue M, Eng C, Amati P, Kraimps JL, Bottani A, Lacombe D, Bonneau D. Longy M, et al. Among authors: amati p. J Med Genet. 1998 Nov;35(11):886-9. doi: 10.1136/jmg.35.11.886. J Med Genet. 1998. PMID: 9832032 Free PMC article.

2

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

Canzian F, Amati P, Harach HR, Kraimps JL, Lesueur F, Barbier J, Levillain P, Romeo G, Bonneau D. Canzian F, et al. Among authors: amati p. Am J Hum Genet. 1998 Dec;63(6):1743-8. doi: 10.1086/302164. Am J Hum Genet. 1998. PMID: 9837827 Free PMC article.

3

A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23.

Amati P, Chomel JC, Nivelon-Chevalier A, Gilgenkrantz S, Kitzis A, Kaplan J, Bonneau D. Amati P, et al. Hum Genet. 1995 Aug;96(2):213-5. doi: 10.1007/BF00207381. Hum Genet. 1995. PMID: 7635472

4

Bilateral cataract and high serum ferritin: a new dominant genetic disorder?

Bonneau D, Winter-Fuseau I, Loiseau MN, Amati P, Berthier M, Oriot D, Beaumont C. Bonneau D, et al. Among authors: amati p. J Med Genet. 1995 Oct;32(10):778-9. doi: 10.1136/jmg.32.10.778. J Med Genet. 1995. PMID: 8558554 Free PMC article.

5

Heterotaxy-neural tube defect and holoprosencephaly occuring independently in two sib fetuses.

Bonneau D, Maréchaud M, Odent S, Piegay I, Godard A, Amati P. Bonneau D, et al. Among authors: amati p. Am J Med Genet. 1999 Jun 4;84(4):373-6. doi: 10.1002/(sici)1096-8628(19990604)84:4<373::aid-ajmg13>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10340655

6

Splenogonadal fusion limb defect syndrome: report of five new cases and review.

Bonneau D, Roume J, Gonzalez M, Toutain A, Carles D, Maréchaud M, Biran-Mucignat V, Amati P, Moraine C. Bonneau D, et al. Among authors: amati p. Am J Med Genet. 1999 Oct 8;86(4):347-58. doi: 10.1002/(sici)1096-8628(19991008)86:4<347::aid-ajmg9>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10494091 Review.

7

Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene.

Kraimps JL, Canzian F, Jost C, Menet E, Amati P, Levillian P, Harach R, Lesueur F, Barbier J, Romeo G, Bonneau D. Kraimps JL, et al. Among authors: amati p. Surgery. 1999 Dec;126(6):1188-94. doi: 10.1067/msy.2099.102606. Surgery. 1999. PMID: 10598206

8

Familial papillary carcinoma of the thyroid.

Kraimps JL, Bouin-Pineau MH, Amati P, Mothes D, Bonneau D, Maréchaud R, Barbier J. Kraimps JL, et al. Among authors: amati p. Surgery. 1997 Jun;121(6):715-8. doi: 10.1016/s0039-6060(97)90063-5. Surgery. 1997. PMID: 9186475 No abstract available.

9

Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

Harach HR, Lesueur F, Amati P, Brown A, Canzian F, Kraimps JL, Levillain P, Menet E, Romeo G, Bonneau D. Harach HR, et al. Among authors: amati p. J Pathol. 1999 Nov;189(3):387-93. doi: 10.1002/(SICI)1096-9896(199911)189:3<387::AID-PATH443>3.0.CO;2-S. J Pathol. 1999. PMID: 10547601

10

A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23.

Amati P, Gasparini P, Zlotogora J, Zelante L, Chomel JC, Kitzis A, Kaplan J, Bonneau D. Amati P, et al. Am J Hum Genet. 1996 May;58(5):1089-92. Am J Hum Genet. 1996. PMID: 8651270 Free PMC article. No abstract available.

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