Fretwell N - Search Results

1

Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males.

Jobling MA, Samara V, Pandya A, Fretwell N, Bernasconi B, Mitchell RJ, Gerelsaikhan T, Dashnyam B, Sajantila A, Salo PJ, Nakahori Y, Disteche CM, Thangaraj K, Singh L, Crawford MH, Tyler-Smith C. Jobling MA, et al. Among authors: fretwell n. Hum Mol Genet. 1996 Nov;5(11):1767-75. doi: 10.1093/hmg/5.11.1767. Hum Mol Genet. 1996. PMID: 8923005

2

Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.

Zerjal T, Dashnyam B, Pandya A, Kayser M, Roewer L, Santos FR, Schiefenhövel W, Fretwell N, Jobling MA, Harihara S, Shimizu K, Semjidmaa D, Sajantila A, Salo P, Crawford MH, Ginter EK, Evgrafov OV, Tyler-Smith C. Zerjal T, et al. Among authors: fretwell n. Am J Hum Genet. 1997 May;60(5):1174-83. Am J Hum Genet. 1997. PMID: 9150165 Free PMC article.

3

Chromosome Y microsatellites: population genetic and evolutionary aspects.

de Knijff P, Kayser M, Caglià A, Corach D, Fretwell N, Gehrig C, Graziosi G, Heidorn F, Herrmann S, Herzog B, Hidding M, Honda K, Jobling M, Krawczak M, Leim K, Meuser S, Meyer E, Oesterreich W, Pandya A, Parson W, Penacino G, Perez-Lezaun A, Piccinini A, Prinz M, Roewer L, et al. de Knijff P, et al. Among authors: fretwell n. Int J Legal Med. 1997;110(3):134-49. doi: 10.1007/s004140050052. Int J Legal Med. 1997. PMID: 9228564

4

Mutation processes at human minisatellites.

Jeffreys AJ, Allen MJ, Armour JA, Collick A, Dubrova Y, Fretwell N, Guram T, Jobling M, May CA, Neil DL, et al. Jeffreys AJ, et al. Among authors: fretwell n. Electrophoresis. 1995 Sep;16(9):1577-85. doi: 10.1002/elps.11501601261. Electrophoresis. 1995. PMID: 8582338 Review.

5

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism.

Monckton DG, Neumann R, Guram T, Fretwell N, Tamaki K, MacLeod A, Jeffreys AJ. Monckton DG, et al. Among authors: fretwell n. Nat Genet. 1994 Oct;8(2):162-70. doi: 10.1038/ng1094-162. Nat Genet. 1994. PMID: 7842015

6

Evaluation of Y-chromosomal STRs: a multicenter study.

Kayser M, Caglià A, Corach D, Fretwell N, Gehrig C, Graziosi G, Heidorn F, Herrmann S, Herzog B, Hidding M, Honda K, Jobling M, Krawczak M, Leim K, Meuser S, Meyer E, Oesterreich W, Pandya A, Parson W, Penacino G, Perez-Lezaun A, Piccinini A, Prinz M, Schmitt C, Roewer L, et al. Kayser M, et al. Among authors: fretwell n. Int J Legal Med. 1997;110(3):125-33, 141-9. doi: 10.1007/s004140050051. Int J Legal Med. 1997. PMID: 9228563

7

A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.

Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilariño Güell C, Aldred M, Brannon CA, Trembath RC, Nichols WC. Machado RD, et al. Among authors: fretwell n. Genomics. 2000 Sep 1;68(2):220-8. doi: 10.1006/geno.2000.6291. Genomics. 2000. PMID: 10964520

8

Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers.

Forman OP, Boursnell ME, Dunmore BJ, Stendall N, van den Sluis B, Fretwell N, Jones C, Wijmenga C, Rothuizen J, van Oost BA, Holmes NG, Binns MM, Jones P. Forman OP, et al. Among authors: fretwell n. Anim Genet. 2005 Dec;36(6):497-501. doi: 10.1111/j.1365-2052.2005.01360.x. Anim Genet. 2005. PMID: 16293123

9

Population structure and inbreeding from pedigree analysis of purebred dogs.

Calboli FC, Sampson J, Fretwell N, Balding DJ. Calboli FC, et al. Among authors: fretwell n. Genetics. 2008 May;179(1):593-601. doi: 10.1534/genetics.107.084954. Genetics. 2008. PMID: 18493074 Free PMC article.

10

Localizing the X-linked orange colour phenotype using feline resource families.

Grahn RA, Lemesch BM, Millon LV, Matise T, Rogers QR, Morris JG, Fretwell N, Bailey SJ, Batt RM, Lyons LA. Grahn RA, et al. Among authors: fretwell n. Anim Genet. 2005 Feb;36(1):67-70. doi: 10.1111/j.1365-2052.2005.01239.x. Anim Genet. 2005. PMID: 15670134

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