137 related articles for article (PubMed ID: 7395868)
21. [Role of the genetically polymorphic systems Pa, Pr and Db in human saliva in forensic medicine].
Sigal ER
Sud Med Ekspert; 1983; 26(1):42-4. PubMed ID: 6836679
[No Abstract] [Full Text] [Related]
22. A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.
Buetow KH; Shiang R; Yang P; Nakamura Y; Lathrop GM; White R; Wasmuth JJ; Wood S; Berdahl LD; Leysens NJ
Am J Hum Genet; 1991 May; 48(5):911-25. PubMed ID: 1673289
[TBL] [Abstract][Full Text] [Related]
23. Genetic polymorphism of PIF proteins in a Japanese population.
Ikemoto S; Tsuchida S; Nishiumi E; Tomita K
Hum Hered; 1987; 37(4):263-4. PubMed ID: 3653906
[TBL] [Abstract][Full Text] [Related]
24. A variant protein in human parotid saliva detected by SDS polyacrylamide gel electrophoresis and its inheritance.
Ikemoto S; Minaguchi K; Tomita K; Suzuki K
Ann Hum Genet; 1979 Jul; 43(1):11-4. PubMed ID: 496391
[TBL] [Abstract][Full Text] [Related]
25. Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.
Litt M; Jorde LB
Am J Hum Genet; 1986 Aug; 39(2):166-78. PubMed ID: 3019131
[TBL] [Abstract][Full Text] [Related]
26. Alleles at the PRH1 locus coding for the human salivary-acidic proline-rich proteins Pa, Db, and PIF.
Azen EA; Kim HS; Goodman P; Flynn S; Maeda N
Am J Hum Genet; 1987 Dec; 41(6):1035-47. PubMed ID: 3687941
[TBL] [Abstract][Full Text] [Related]
27. A simplified procedure for simultaneous detection of salivary proteins and its application in paternity testing.
Caeiro JL; Boán F; Carracedo A
Forensic Sci Int; 1987 Jan; 33(1):47-52. PubMed ID: 3469132
[TBL] [Abstract][Full Text] [Related]
28. Multipoint mapping studies of six loci on chromosome 11.
Meyers DA; Beaty TH; Maestri NE; Kittur SD; Antonarakis SE; Kazazian HH
Hum Hered; 1987; 37(2):94-101. PubMed ID: 3294571
[TBL] [Abstract][Full Text] [Related]
29. Genetic polymorphisms of the human parotid salivary proteins and isoenzymes among the Japanese population.
Ikemoto S; Tsuchida S; Hinohara H; Nishiumi A; Tomita K
Acta Med Leg Soc (Liege); 1985; 35(2):169-75. PubMed ID: 2485112
[No Abstract] [Full Text] [Related]
30. Isolation and partial characterization of a polymorphic protein (Pm) in human parotid saliva.
Minaguchi K; Ikemoto S; Suzuki K
Biochem Genet; 1981 Jun; 19(5-6):617-21. PubMed ID: 7295289
[No Abstract] [Full Text] [Related]
31. Studies of genetic markers in human saliva. (VII). Frequencies of the major parotid salivary glycoprotein (GI) system in a Japanese population.
Minaguchi K; Takaesu Y; Tsutsumi T; Suzuki K
Bull Tokyo Dent Coll; 1981 Feb; 22(1):1-6. PubMed ID: 6940681
[No Abstract] [Full Text] [Related]
32. Deletion and linkage mapping of eight markers from the proximal short arm of chromosome 6.
Zoghbi HY; Ballantyne CM; O'Brien WE; McCall AE; Kwiatkowski TJ; Ledbetter SA; Beaudet AL
Genomics; 1990 Feb; 6(2):352-7. PubMed ID: 1968423
[TBL] [Abstract][Full Text] [Related]
33. Genetic polymorphisms of the Pmo1 and Pmo2 salivary proteins detected by the modified protein staining method.
Minaguchi K; Suzuki K
Ann Hum Genet; 1988 Jul; 52(3):177-87. PubMed ID: 3250329
[TBL] [Abstract][Full Text] [Related]
34. Studies of genetic markers in human saliva. (I). Frequencies of Pa and Pb systems from parotid saliva of Japanese in Tokyo.
Minaguchi K; Ikemoto S; Nakajima I; Suzuki K
Bull Tokyo Dent Coll; 1976 Nov; 17(4):185-90. PubMed ID: 1076070
[No Abstract] [Full Text] [Related]
35. Linkage disequilibrium analyses and restriction mapping of four RFLPs at the pro alpha 2(I) collagen locus: lack of correlation between linkage disequilibrium and physical distance.
Børresen AL; Møller P; Berg K
Hum Genet; 1988 Mar; 78(3):216-21. PubMed ID: 2894343
[TBL] [Abstract][Full Text] [Related]
36. Linkage analysis of pure depressive disease.
Tanna VL; Wilson AF; Winokur G; Elston RC
J Psychiatr Res; 1989; 23(2):99-107. PubMed ID: 2585349
[TBL] [Abstract][Full Text] [Related]
37. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
Lesko JG; Lewis RA; Nussbaum RL
Am J Hum Genet; 1987 Apr; 40(4):303-11. PubMed ID: 2883887
[TBL] [Abstract][Full Text] [Related]
38. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
Thibodeau SN; Dorkins HR; Faulk KR; Berry R; Smith AC; Hagerman R; King A; Davies KE
Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993
[TBL] [Abstract][Full Text] [Related]
39. Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.
Chen JD; Halliday F; Keith G; Sheffield L; Dickinson P; Gray R; Constable I; Denton M
Am J Hum Genet; 1989 Sep; 45(3):401-11. PubMed ID: 2570529
[TBL] [Abstract][Full Text] [Related]
40. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
Ramoz N; Reichert JG; Smith CJ; Silverman JM; Bespalova IN; Davis KL; Buxbaum JD
Am J Psychiatry; 2004 Apr; 161(4):662-9. PubMed ID: 15056512
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]