Amos J - Search Results

1

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients.

Dean M, White MB, Amos J, Gerrard B, Stewart C, Khaw KT, Leppert M. Dean M, et al. Among authors: amos j. Cell. 1990 Jun 1;61(5):863-70. doi: 10.1016/0092-8674(90)90196-l. Cell. 1990. PMID: 2344617

2

A 22-bp deletion in the coding region of the cystic fibrosis gene.

Dean M, White MB, Gerrard B, Milunsky A, Amos J. Dean M, et al. Among authors: amos j. Genomics. 1992 May;13(1):235-6. doi: 10.1016/0888-7543(92)90233-i. Genomics. 1992. PMID: 1374361 No abstract available.

3

A frame-shift mutation in the cystic fibrosis gene.

White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M. White MB, et al. Among authors: amos j. Nature. 1990 Apr 12;344(6267):665-7. doi: 10.1038/344665a0. Nature. 1990. PMID: 1691449

4

Identification of cystic fibrosis mutations.

Dean M, Gerrard B, Stewart C, Krueger L, Holsclaw D, Quittell L, Baranov V, Kapronov N, Leppert M, Amos J, et al. Dean M, et al. Among authors: amos j. Adv Exp Med Biol. 1991;290:45-51. doi: 10.1007/978-1-4684-5934-0_6. Adv Exp Med Biol. 1991. PMID: 1719771 No abstract available.

5

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.

Anguiano A, Oates RD, Amos JA, Dean M, Gerrard B, Stewart C, Maher TA, White MB, Milunsky A. Anguiano A, et al. Among authors: amos ja. JAMA. 1992 Apr 1;267(13):1794-7. JAMA. 1992. PMID: 1545465

6

Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8.

Dean M, Amos JA, Lynch J, Romeo G, Devoto M, Ward K, Halley D, Oostra B, Ferrari M, Russo S, et al. Dean M, et al. Among authors: amos ja. Hum Genet. 1990 Aug;85(3):275-8. doi: 10.1007/BF00206745. Hum Genet. 1990. PMID: 1975555 Free article.

7

Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis.

Dean M, O'Connell P, Leppert M, Park M, Amos JA, Phillips DG, White R, Vande Woude GF. Dean M, et al. Among authors: amos ja. J Pediatr. 1987 Oct;111(4):490-5. doi: 10.1016/s0022-3476(87)80106-3. J Pediatr. 1987. PMID: 2888841 Free article.

8

A universal array-based multiplexed test for cystic fibrosis carrier screening.

Amos JA, Bridge-Cook P, Ponek V, Jarvis MR. Amos JA, et al. Expert Rev Mol Diagn. 2006 Jan;6(1):15-22. doi: 10.1586/14737159.6.1.15. Expert Rev Mol Diagn. 2006. PMID: 16359263

9

Cystic fibrosis.

Lewis MJ, Lewis EH 3rd, Amos JA, Tsongalis GJ. Lewis MJ, et al. Among authors: amos ja. Am J Clin Pathol. 2003 Dec;120 Suppl:S3-13. doi: 10.1309/DUUVFR11W595V7FE. Am J Clin Pathol. 2003. PMID: 15298139 Review.

10

DNA analysis of cystic fibrosis genotypes in relatives with equivocal sweat test results.

Amos JA, Janes SR, Erbe RW. Amos JA, et al. Clin Invest Med. 1990 Feb;13(1):1-5. Clin Invest Med. 1990. PMID: 2311311

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