Smith S - Search Results

1

Four polymorphic microsatellite loci for the European wild rabbit, Oryctolagus cuniculus.

Rico C, Rico I, Webb N, Smith S, Bell D, Hewitt G. Rico C, et al. Among authors: smith s. Anim Genet. 1994 Oct;25(5):367. doi: 10.1111/j.1365-2052.1994.tb00379.x. Anim Genet. 1994. PMID: 7818179 No abstract available.

2

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness.

Jin H, May M, Tranebjaerg L, Kendall E, Fontán G, Jackson J, Subramony SH, Arena F, Lubs H, Smith S, Stevenson R, Schwartz C, Vetrie D. Jin H, et al. Among authors: smith s. Nat Genet. 1996 Oct;14(2):177-80. doi: 10.1038/ng1096-177. Nat Genet. 1996. PMID: 8841189

3

Complex patterns of intragenic polymorphism at the PDGFA locus.

Bonthron DT, Smith SJ, Campbell R. Bonthron DT, et al. Among authors: smith sj. Hum Genet. 1999 Nov;105(5):452-9. doi: 10.1007/s004390051130. Hum Genet. 1999. PMID: 10598812

4

The EUROGEM map of human chromosome 7.

Badbanchi F, Otto M, Kohlhauer U, Grzeschik N, Beck S, Smith SJ, Swallow DM, Kooy RF, Vergnaud G, Aldred M, et al. Badbanchi F, et al. Among authors: smith sj. Eur J Hum Genet. 1994;2(3):216-7. Eur J Hum Genet. 1994. PMID: 7834287 No abstract available.

5

De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Bonthron DT, Smith SJ, Fantes J, Gosden CM. Bonthron DT, et al. Among authors: smith sj. Am J Hum Genet. 1993 Sep;53(3):629-37. Am J Hum Genet. 1993. PMID: 8352273 Free PMC article.

6

Physical and genetic mapping at the ATA/ATC locus on chromosome 11q22-23.

Rotman G, Savitski K, Vanagaite L, Bar-Shira A, Ziv Y, Gilad S, Uchenik V, Smith S, Shiloh Y. Rotman G, et al. Among authors: smith s. Int J Radiat Biol. 1994 Dec;66(6 Suppl):S63-6. Int J Radiat Biol. 1994. PMID: 7836854

7

Predominance of null mutations in ataxia-telangiectasia.

Gilad S, Khosravi R, Shkedy D, Uziel T, Ziv Y, Savitsky K, Rotman G, Smith S, Chessa L, Jorgensen TJ, Harnik R, Frydman M, Sanal O, Portnoi S, Goldwicz Z, Jaspers NG, Gatti RA, Lenoir G, Lavin MF, Tatsumi K, Wegner RD, Shiloh Y, Bar-Shira A. Gilad S, et al. Among authors: smith s. Hum Mol Genet. 1996 Apr;5(4):433-9. doi: 10.1093/hmg/5.4.433. Hum Mol Genet. 1996. PMID: 8845835 Free article.

8

Skewed sex ratios in familial holoprosencephaly and in people with isolated single maxillary central incisor.

Suthers G, Smith S, Springbett S. Suthers G, et al. Among authors: smith s. J Med Genet. 1999 Dec;36(12):924-6. J Med Genet. 1999. PMID: 10594002 Free PMC article.

9

Familial inverted duplication 7p.

Schaefer GB, Novak K, Steele D, Buehler B, Smith S, Zaleski D, Pickering D, Nelson M, Sanger W. Schaefer GB, et al. Among authors: smith s. Am J Med Genet. 1995 Mar 27;56(2):184-7. doi: 10.1002/ajmg.1320560214. Am J Med Genet. 1995. PMID: 7542835 Review.

10

Virtual discharge counseling: An assessment of scalability of a novel patient educational process across a multi-site urban emergency department.

Leybov V, Ross J, Grabinski Z, Smith SW, Wang Y, Wittman IG, Caspers CG, Tse AB, Conroy N. Leybov V, et al. Among authors: smith sw. J Telemed Telecare. 2024 Nov 18:1357633X241297337. doi: 10.1177/1357633X241297337. Online ahead of print. J Telemed Telecare. 2024. PMID: 39558591

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