Warren ST - Search Results

1

Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.

Gorlin JB, Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ. Gorlin JB, et al. Among authors: warren st. Genomics. 1993 Aug;17(2):496-8. doi: 10.1006/geno.1993.1354. Genomics. 1993. PMID: 8406501

2

Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.

Consalez GG, Stayton CL, Freimer NB, Goonewardena P, Brown WT, Gilliam TC, Warren ST. Consalez GG, et al. Among authors: warren st. Genomics. 1992 Apr;12(4):710-4. doi: 10.1016/0888-7543(92)90299-8. Genomics. 1992. PMID: 1572645

3

Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel.

Traupe H, van den Ouweland AM, van Oost BA, Vogel W, Vetter U, Warren ST, Rocchi M, Darlison MG, Ropers HH. Traupe H, et al. Among authors: warren st. Genomics. 1992 Jun;13(2):481-3. doi: 10.1016/0888-7543(92)90279-2. Genomics. 1992. PMID: 1612609

4

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.

Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke P, Raeymaekers P, Van Broeckhoven C, Consalez GG, Freeman SB, Warren ST, et al. Willems PJ, et al. Among authors: warren st. Genomics. 1990 Oct;8(2):367-70. doi: 10.1016/0888-7543(90)90294-5. Genomics. 1990. PMID: 1979056

5

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ. van den Ouweland AM, et al. Among authors: warren st. Hum Mol Genet. 1994 Oct;3(10):1823-7. doi: 10.1093/hmg/3.10.1823. Hum Mol Genet. 1994. PMID: 7849707

6

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

Kunst CB, Warren ST. Kunst CB, et al. Among authors: warren st. Cell. 1994 Jun 17;77(6):853-61. doi: 10.1016/0092-8674(94)90134-1. Cell. 1994. PMID: 7911740

7

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Ashley CT, et al. Among authors: warren st. Nat Genet. 1993 Jul;4(3):244-51. doi: 10.1038/ng0793-244. Nat Genet. 1993. PMID: 8358432

8

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease.

Bione S, Small K, Aksmanovic VM, D'Urso M, Ciccodicola A, Merlini L, Morandi L, Kress W, Yates JR, Warren ST, et al. Bione S, et al. Among authors: warren st. Hum Mol Genet. 1995 Oct;4(10):1859-63. doi: 10.1093/hmg/4.10.1859. Hum Mol Genet. 1995. PMID: 8595407

9

The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.

Kunst CB, Leeflang EP, Iber JC, Arnheim N, Warren ST. Kunst CB, et al. Among authors: warren st. J Med Genet. 1997 Aug;34(8):627-31. doi: 10.1136/jmg.34.8.627. J Med Genet. 1997. PMID: 9279752 Free PMC article.

10

Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region.

van den Ouweland AM, Knoop MT, Knoers VV, Markslag PW, Rocchi M, Warren ST, Ropers HH, Fahrenholz F, Monnens LA, van Oost BA. van den Ouweland AM, et al. Among authors: warren st. Genomics. 1992 Aug;13(4):1350-2. doi: 10.1016/0888-7543(92)90067-3. Genomics. 1992. PMID: 1324225

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

215 results

Search Page

Filters