Oddoux C - Search Results

1

High-level inducible expression of visual pigments in transfected cells.

Kazmi MA, Dubin RA, Oddoux C, Ostrer H. Kazmi MA, et al. Among authors: oddoux c. Biotechniques. 1996 Aug;21(2):304-11. doi: 10.2144/96212rr05. Biotechniques. 1996. PMID: 8862817 Free article.

2

X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome.

Sculerati N, Perle MA, Oddoux C, Clayton CM, Ostrer H. Sculerati N, et al. Among authors: oddoux c. Otolaryngol Head Neck Surg. 1997 Dec;117(6):S221-5. doi: 10.1016/S0194-59989770108-6. Otolaryngol Head Neck Surg. 1997. PMID: 9419154 No abstract available.

3

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%.

Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. Oddoux C, et al. Nat Genet. 1996 Oct;14(2):188-90. doi: 10.1038/ng1096-188. Nat Genet. 1996. PMID: 8841192

4

Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.

Wistinghausen B, Reischer A, Oddoux C, Ostrer H, Nardi M, Karpatkin M. Wistinghausen B, et al. Among authors: oddoux c. Br J Haematol. 1997 Dec;99(3):575-7. doi: 10.1046/j.1365-2141.1997.4343244.x. Br J Haematol. 1997. PMID: 9401068 Free article.

5

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM, Nelson H, Sarafoglou K, McCain N, Peretz H, Seligsohn U, Luzzatto L, Nafa K, Nardi M, Karpatkin M, Aksentijevich I, Kastner D, Axelrod F, Ostrer H. Oddoux C, et al. J Clin Endocrinol Metab. 1999 Dec;84(12):4405-9. doi: 10.1210/jcem.84.12.6268. J Clin Endocrinol Metab. 1999. PMID: 10599695 Review.

6

The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects.

Fitzgerald T, Duva S, Ostrer H, Pass K, Oddoux C, Ruben R, Caggana M. Fitzgerald T, et al. Among authors: oddoux c. Clin Genet. 2004 Apr;65(4):338-42. doi: 10.1111/j.1399-0004.2004.00233.x. Clin Genet. 2004. PMID: 15025729

7

Prenatal diagnostic testing for familial dysautonomia using linked genetic markers.

Oddoux C, Reich E, Axelrod F, Blumenfeld A, Maayan C, Slaugenhaupt S, Gusella J, Ostrer H. Oddoux C, et al. Prenat Diagn. 1995 Sep;15(9):817-26. doi: 10.1002/pd.1970150905. Prenat Diagn. 1995. PMID: 8559751

8

TbetaR-I(6A) is a candidate tumor susceptibility allele.

Pasche B, Kolachana P, Nafa K, Satagopan J, Chen YG, Lo RS, Brener D, Yang D, Kirstein L, Oddoux C, Ostrer H, Vineis P, Varesco L, Jhanwar S, Luzzatto L, Massagué J, Offit K. Pasche B, et al. Among authors: oddoux c. Cancer Res. 1999 Nov 15;59(22):5678-82. Cancer Res. 1999. PMID: 10582683

9

The impact of Converso Jews on the genomes of modern Latin Americans.

Velez C, Palamara PF, Guevara-Aguirre J, Hao L, Karafet T, Guevara-Aguirre M, Pearlman A, Oddoux C, Hammer M, Burns E, Pe'er I, Atzmon G, Ostrer H. Velez C, et al. Among authors: oddoux c. Hum Genet. 2012 Feb;131(2):251-63. doi: 10.1007/s00439-011-1072-z. Epub 2011 Jul 26. Hum Genet. 2012. PMID: 21789512

10

Response to Zlotogora and Meiner.

Baskovich B, Hiraki S, Oddoux C, Ostrer H, Upadhyay K. Baskovich B, et al. Among authors: oddoux c. Genet Med. 2016 May;18(5):530. doi: 10.1038/gim.2015.170. Epub 2015 Dec 10. Genet Med. 2016. PMID: 26656652 Free article. No abstract available.

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