130 related articles for article (PubMed ID: 7328306)
21. 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. PubMed ID: 7849405
[No Abstract] [Full Text] [Related]
22. Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse.
Marks SC; Seifert MF; Lane PW
J Hered; 1985; 76(3):171-6. PubMed ID: 3998439
[TBL] [Abstract][Full Text] [Related]
23. Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2.
Juriloff DM; Harris MJ
J Hered; 1991; 82(5):402-5. PubMed ID: 1940283
[TBL] [Abstract][Full Text] [Related]
24. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
Cho KI; Lee JW; Kim KS; Lee EJ; Suh JG; Lee HJ; Kim HT; Hong SH; Chung WH; Chang KT; Hyun BH; Oh YS; Ryoo ZY
Comp Med; 2003 Dec; 53(6):642-8. PubMed ID: 14727813
[TBL] [Abstract][Full Text] [Related]
25. Linkage relationships in domestic fowl.
Somes RG
J Hered; 1973; 64(4):217-21. PubMed ID: 4766209
[No Abstract] [Full Text] [Related]
26. X-linked polydactyly (Xpl), a new mutation in the mouse.
Sweet HO; Lane PW
J Hered; 1980; 71(3):207-9. PubMed ID: 7391545
[TBL] [Abstract][Full Text] [Related]
27. Identification of novel genetic loci for bone size and mechanosensitivity in an ENU mutant exhibiting decreased bone size.
Srivastava AK; Kapur S; Mohan S; Yu H; Kapur S; Wergedal J; Baylink DJ
J Bone Miner Res; 2005 Jun; 20(6):1041-50. PubMed ID: 15883645
[TBL] [Abstract][Full Text] [Related]
28. Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci.
Watson ML; Rao JK; Gilkeson GS; Ruiz P; Eicher EM; Pisetsky DS; Matsuzawa A; Rochelle JM; Seldin MF
J Exp Med; 1992 Dec; 176(6):1645-56. PubMed ID: 1460423
[TBL] [Abstract][Full Text] [Related]
29. Genetic and physical delineation of the region of the mouse deafness mutation shaker-2.
Wakabayashi Y; Kikkawa Y; Matsumoto Y; Shinbo T; Kosugi S; Chou D; Furuya M; Jishage K; Noda T; Yonekawa H; Kominami R
Biochem Biophys Res Commun; 1997 May; 234(1):107-10. PubMed ID: 9168970
[TBL] [Abstract][Full Text] [Related]
30. Cerebellar deficient folia (cdf): a new mutation on mouse chromosome 6.
Cook SA; Bronson RT; Donahue LR; Ben-Arie N; Davisson MT
Mamm Genome; 1997 Feb; 8(2):108-12. PubMed ID: 9060409
[TBL] [Abstract][Full Text] [Related]
31. Dominant lethality of the mouse skeletal mutation tail-short (Ts) is determined by the Ts allele from mating partners.
Ishijima J; Yasui H; Morishima M; Shiroishi T
Genomics; 1998 May; 49(3):341-50. PubMed ID: 9615218
[TBL] [Abstract][Full Text] [Related]
32. Linkage of gold, its recessive lethality and sex-related variation in crossing-over in Culex pipiens (Diptera: Culicidae).
McCelland GA; Smithson TW
Can J Genet Cytol; 1968 Jun; 10(2):374-84. PubMed ID: 5699833
[No Abstract] [Full Text] [Related]
33. The genetic analysis of a reciprocal translocation, eT1(III; V), in Caenorhabditis elegans.
Rosenbluth RE; Baillie DL
Genetics; 1981; 99(3-4):415-28. PubMed ID: 6953041
[TBL] [Abstract][Full Text] [Related]
34. Molecular mapping of the mouse db mutation.
Bahary N; Leibel RL; Joseph L; Friedman JM
Proc Natl Acad Sci U S A; 1990 Nov; 87(21):8642-6. PubMed ID: 1978328
[TBL] [Abstract][Full Text] [Related]
35. The mouse mutation claw paw: forelimb deformity and delayed myelination throughout the peripheral nervous system.
Henry EW; Eicher EM; Sidman RL
J Hered; 1991; 82(4):287-94. PubMed ID: 1652607
[TBL] [Abstract][Full Text] [Related]
36. Rachiterata: a new skeletal mutation on chromosome 2 of the mouse.
Varnum DS; Stevens LC
J Hered; 1974; 65(2):91-3. PubMed ID: 4837306
[No Abstract] [Full Text] [Related]
37. Two kinds of ENU-induced scant hair mice and mapping of the mutant genes.
Wu BJ; Shao YX; Mao HH; Tang D; Liu J; Xue ZF; Li HD
J Dermatol Sci; 2004 Dec; 36(3):149-56. PubMed ID: 15541636
[TBL] [Abstract][Full Text] [Related]
38. Linkage of faded gene (fe) to chromosome 6 of the mouse.
Oh YS; Tomita T
Jikken Dobutsu; 1987 Jan; 36(1):73-7. PubMed ID: 3816991
[TBL] [Abstract][Full Text] [Related]
39. Rostral cerebellar malformation, (rcm): a new recessive mutation on chromosome 3 of the mouse.
Lane PW; Bronson RT; Spencer CA
J Hered; 1992; 83(4):315-8. PubMed ID: 1401878
[TBL] [Abstract][Full Text] [Related]
40. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16.
Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet JL
Genomics; 1994 Jan; 19(1):9-11. PubMed ID: 8188247
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]