Stanier P - Search Results

1

Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications.

Scambler PJ, Wainwright BJ, Farrall M, Bell J, Stanier P, Lench NJ, Bell G, Kruyer H, Ramirez F, Williamson R. Scambler PJ, et al. Among authors: stanier p. Lancet. 1985 Nov 30;2(8466):1241-2. doi: 10.1016/s0140-6736(85)90765-2. Lancet. 1985. PMID: 2866313 No abstract available.

2

First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes.

Farrall M, Law HY, Rodeck CH, Warren R, Stanier P, Super M, Lissens W, Scambler P, Watson E, Wainwright B, et al. Farrall M, et al. Among authors: stanier p. Lancet. 1986 Jun 21;1(8495):1402-5. doi: 10.1016/s0140-6736(86)91553-9. Lancet. 1986. PMID: 2872515

3

Simple non-invasive method to obtain DNA for gene analysis.

Lench N, Stanier P, Williamson R. Lench N, et al. Among authors: stanier p. Lancet. 1988 Jun 18;1(8599):1356-8. doi: 10.1016/s0140-6736(88)92178-2. Lancet. 1988. PMID: 2898042

4

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

Tata F, Stanier P, Wicking C, Halford S, Kruyer H, Lench NJ, Scambler PJ, Hansen C, Braman JC, Williamson R, et al. Tata F, et al. Among authors: stanier p. Genomics. 1991 Jun;10(2):301-7. doi: 10.1016/0888-7543(91)90312-3. Genomics. 1991. PMID: 1712752

5

Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus.

Stanier P, Estivill X, Lench N, Williamson R. Stanier P, et al. Hum Genet. 1988 Nov;80(3):309-10. doi: 10.1007/BF01790107. Hum Genet. 1988. PMID: 2461342

6

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.

Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KM, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P, et al. Estivill X, et al. Among authors: stanier p. Nature. 1987 Apr 30-May 6;326(6116):840-5. doi: 10.1038/326840a0. Nature. 1987. PMID: 2883581

7

The application of molecular genetics to the study of the basic defect causing cystic fibrosis.

Estivill X, Bates G, Bell G, Farrall M, Frederick P, Hawley K, Kruyer H, Lench N, Scrambler P, Stanier P, et al. Estivill X, et al. Among authors: stanier p. Prog Clin Biol Res. 1987;254:181-90. Prog Clin Biol Res. 1987. PMID: 2893385 Review.

8

Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes.

Law HY, Stanier P, Williamson R, Modell B, Ward RH, Petrou M, Old J, Farrall M. Law HY, et al. Among authors: stanier p. Prenat Diagn. 1987 Mar;7(3):215-21. doi: 10.1002/pd.1970070309. Prenat Diagn. 1987. PMID: 3588540

9

Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless.

Wainwright BJ, Scambler PJ, Stanier P, Watson EK, Bell G, Wicking C, Estivill X, Courtney M, Boue A, Pedersen PS, et al. Wainwright BJ, et al. Among authors: stanier p. EMBO J. 1988 Jun;7(6):1743-8. doi: 10.1002/j.1460-2075.1988.tb03003.x. EMBO J. 1988. PMID: 2971536 Free PMC article.

10

Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects.

Newton R, Stanier P, Loughna S, Henderson DJ, Forbes SA, Farrall M, Jensson O, Moore GE. Newton R, et al. Among authors: stanier p. Clin Genet. 1994 May;45(5):241-9. doi: 10.1111/j.1399-0004.1994.tb04149.x. Clin Genet. 1994. PMID: 8076409

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