Gerrard B - Search Results

1

Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8.

Iannuzzi MC, Dean M, Drumm ML, Hidaka N, Cole JL, Perry A, Stewart C, Gerrard B, Collins FS. Iannuzzi MC, et al. Among authors: gerrard b. Am J Hum Genet. 1989 May;44(5):695-703. Am J Hum Genet. 1989. PMID: 2565081 Free PMC article.

2

Two frameshift mutations in the cystic fibrosis gene.

Iannuzzi MC, Stern RC, Collins FS, Hon CT, Hidaka N, Strong T, Becker L, Drumm ML, White MB, Gerrard B, et al. Iannuzzi MC, et al. Among authors: gerrard b. Am J Hum Genet. 1991 Feb;48(2):227-31. Am J Hum Genet. 1991. PMID: 1990834 Free PMC article.

3

Approaches to localizing disease genes as applied to cystic fibrosis.

Dean M, Drumm ML, Stewart C, Gerrard B, Perry A, Hidaka N, Cole JL, Collins FS, Iannuzzi MC. Dean M, et al. Among authors: gerrard b. Nucleic Acids Res. 1990 Jan 25;18(2):345-50. doi: 10.1093/nar/18.2.345. Nucleic Acids Res. 1990. PMID: 1970161 Free PMC article.

4

Genetic markers for oncogenes, growth factors, and cystic fibrosis.

Dean M, Stewart C, Perry A, Gerrard B, Beck T, Rapp U, Drumm M, Iannuzzi M, Collins F, O'Brien S. Dean M, et al. Among authors: gerrard b. Haematol Blood Transfus. 1989;32:360-5. doi: 10.1007/978-3-642-74621-5_63. Haematol Blood Transfus. 1989. PMID: 2576235 No abstract available.

5

Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations.

Claustres M, Gerrard B, Kjellberg P, Desgeorges M, Demaille J, Dean M. Claustres M, et al. Among authors: gerrard b. Hum Mutat. 1992;1(4):310-3. doi: 10.1002/humu.1380010408. Hum Mutat. 1992. PMID: 1284537

6

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: gerrard b. JAMA. 1992 Apr 1;267(13):1794-7. JAMA. 1992. PMID: 1545465

7

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: gerrard b. Nature. 1990 Apr 12;344(6267):665-7. doi: 10.1038/344665a0. Nature. 1990. PMID: 1691449

8

A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene.

White MB, Leppert M, Nielsen D, Zielenski J, Gerrard B, Stewart C, Dean M. White MB, et al. Among authors: gerrard b. Genomics. 1991 Nov;11(3):778-9. doi: 10.1016/0888-7543(91)90092-s. Genomics. 1991. PMID: 1723056 No abstract available.

9

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: gerrard b. Cell. 1990 Jun 1;61(5):863-70. doi: 10.1016/0092-8674(90)90196-l. Cell. 1990. PMID: 2344617

10

Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database.

Allikmets R, Gerrard B, Hutchinson A, Dean M. Allikmets R, et al. Among authors: gerrard b. Hum Mol Genet. 1996 Oct;5(10):1649-55. doi: 10.1093/hmg/5.10.1649. Hum Mol Genet. 1996. PMID: 8894702

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