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Items: 1 to 20 of 91

1.

The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization.

Uwechue IC, Cooper BF, Goble C, Hacker T, Blair HJ, Burke DT, Herman G, Boyd Y.

Genomics. 1996 Oct 15;37(2):238-41.

PMID:
8921395
2.

Chromosomal mapping and developmental study of Tattered-Hokkaido (Tdho).

Seo KW, Miyoshi H, Kon Y, Watanabe T.

Mamm Genome. 1997 Aug;8(8):578-80.

PMID:
9250864
3.

Faint lined (Fnl): a novel X-linked coat mutant in the mouse.

Gormally E, Boyd Y.

Genet Res. 1998 Dec;72(3):211-6.

PMID:
10036977
4.

Genetic analyses of tattered, an X-linked dominant, developmental mouse mutation.

Merrell K, Gonzales JC, Wells S, Calame K, Herman GE.

Mamm Genome. 1995 Apr;6(4):291-4.

PMID:
7613037
5.

High-resolution comparative mapping of the proximal region of the mouse X chromosome.

Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y.

Genomics. 1995 Jul 20;28(2):305-10.

PMID:
8530041
6.

Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

Derry JM, Gormally E, Means GD, Zhao W, Meindl A, Kelley RI, Boyd Y, Herman GE.

Nat Genet. 1999 Jul;22(3):286-90.

PMID:
10391218
7.

Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.

Korobova O, Lane PW, Perry J, Palmer S, Ashworth A, Davisson MT, Arnheim N.

Genomics. 1998 Dec 15;54(3):556-9.

PMID:
9878259
8.

The mouse scurfy (sf) mutation is tightly linked to Gata1 and Tfe3 on the proximal X chromosome.

Blair PJ, Carpenter DA, Godfrey VL, Russell LB, Wilkinson JE, Rinchik EM.

Mamm Genome. 1994 Oct;5(10):652-4. No abstract available.

PMID:
7849405
9.
10.

Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice.

Juriloff DM, Harris MJ, Banks KG, Mah DG.

Mamm Genome. 2000 Jun;11(6):440-7.

PMID:
10818208
11.

Cataract mutations and lens development.

Graw J.

Prog Retin Eye Res. 1999 Mar;18(2):235-67. Review.

PMID:
9932285
12.
14.
15.

Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.

Walder RY, Shalev H, Brennan TM, Carmi R, Elbedour K, Scott DA, Hanauer A, Mark AL, Patil S, Stone EM, Sheffield VC.

Hum Mol Genet. 1997 Sep;6(9):1491-7.

16.

The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase.

Liu XY, Dangel AW, Kelley RI, Zhao W, Denny P, Botcherby M, Cattanach B, Peters J, Hunsicker PR, Mallon AM, Strivens MA, Bate R, Miller W, Rhodes M, Brown SD, Herman GE.

Nat Genet. 1999 Jun;22(2):182-7.

PMID:
10369263
17.

Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.

Candille SI, Pardue MT, McCall MA, Peachey NS, Gregg RG.

Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2748-51.

PMID:
10509675
18.

exma: an X-linked insertional mutation that disrupts forebrain and eye development.

Cunningham D, Xiao Q, Chatterjee A, Sulik K, Juriloff D, Elder F, Harrison W, Schuster G, Overbeek PA, Herman GE.

Mamm Genome. 2002 Apr;13(4):179-85.

PMID:
11956759
19.

Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome.

Ko MS, Threat TA, Wang X, Horton JH, Cui Y, Wang X, Pryor E, Paris J, Wells-Smith J, Kitchen JR, Rowe LB, Eppig J, Satoh T, Brant L, Fujiwara H, Yotsumoto S, Nakashima H.

Hum Mol Genet. 1998 Nov;7(12):1967-78.

20.

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, Scheffer I, Berkovic S, Scaravilli F, King RA, Ledbetter DH, Schlessinger D, Dobyns WB, Walsh CA.

Hum Mol Genet. 1997 Apr;6(4):555-62.

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