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Items: 1 to 20 of 121

1.

Single gene inheritance of occurrence of head spots in mice.

Wildman J, Doolittle DP.

J Hered. 1986 Mar-Apr;77(2):136-8.

PMID:
3458810
2.

Quantitative genetics of age-related retinal degeneration: a second F1 intercross between the A/J and C57BL/6 strains.

Danciger M, Yang H, Ralston R, Liu Y, Matthes MT, Peirce J, Lavail MM.

Mol Vis. 2007 Jan 25;13:79-85.

PMID:
17277741
3.

Quantitative trait loci that modify the severity of spotting in piebald mice.

Pavan WJ, Mac S, Cheng M, Tilghman SM.

Genome Res. 1995 Aug;5(1):29-41.

PMID:
8717053
4.

Mapping of the azh locus to mouse chromosome 4.

Meistrich ML, Trostle-Weige PK, Womack JE.

J Hered. 1992 Jan-Feb;83(1):56-61.

PMID:
1552159
5.

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
6.

Locating salmonella resistance gene on mouse chromosome 1.

Plant J, Glynn AA.

Clin Exp Immunol. 1979 Jul;37(1):1-6.

PMID:
385184
7.

Mapping of new recessive cataract gene (lr2) in the mouse.

Song CW, Okumoto M, Mori N, Kim JS, Han SS, Esaki K.

Mamm Genome. 1997 Dec;8(12):927-31.

PMID:
9383287
8.

Cleft palate: more genetic lessons from mice.

Juriloff DM, Harris MJ.

J Craniofac Genet Dev Biol. 1988;8(2):127-34.

PMID:
3182968
9.

Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse.

Hollander WF.

J Hered. 1981 Sep-Oct;72(5):358-9.

PMID:
7328306
10.

Crosses of NOD mice with the related NON strain. A polygenic model for IDDM.

McAleer MA, Reifsnyder P, Palmer SM, Prochazka M, Love JM, Copeman JB, Powell EE, Rodrigues NR, Prins JB, Serreze DV, et al.

Diabetes. 1995 Oct;44(10):1186-95.

PMID:
7556956
11.

Simulation of the distribution of parental strains' genomes in RC strains of mice.

Moen CJ, Stoffers HJ, Hart AA, Westerhoff HV, Demant P.

Mamm Genome. 1997 Dec;8(12):884-9.

PMID:
9383279
13.
14.

Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes.

Cryns K, Van Spaendonck MP, Flothmann K, van Alphen AM, Van De Heyning PH, Timmermans JP, De Zeeuw CI, Van Camp G.

Genome Res. 2002 Apr;12(4):613-7.

PMID:
11932245
15.

Recombinant congenic strains of mice from B10.D2 and DBA/2: their contribution to behavior genetic research and application to audiogenic seizures.

Martin B, Marchaland C, Phillips J, Chapouthier G, Spach C, Motta R.

Behav Genet. 1992 Nov;22(6):685-701.

PMID:
1290454
16.

Simultaneous selection of major and minor genes: use of QTL to increase selection efficiency of coleoptile length of wheat (Triticum aestivum L.).

Wang J, Chapman SC, Bonnett DG, Rebetzke GJ.

Theor Appl Genet. 2009 Jun;119(1):65-74. doi: 10.1007/s00122-009-1017-2. Epub 2009 Apr 10.

PMID:
19360392
17.

Chromosome substitution strains: a new way to study genetically complex traits.

Hill AE, Lander ES, Nadeau JH.

Methods Mol Med. 2006;128:153-72.

PMID:
17071995
18.
19.

Marker assisted selection for the improvement of two antagonistic traits under mixed inheritance.

Verrier E.

Genet Sel Evol. 2001 Jan-Feb;33(1):17-38.

PMID:
11268312
20.

Major gene determination of liability to spontaneous cleft lip in the mouse.

Biddle FG, Fraser FC.

J Craniofac Genet Dev Biol Suppl. 1986;2:67-88.

PMID:
3491126

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