These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
30. Two dinucleotide repeat polymorphisms at 21q22.3 (D21S416 and D21S1235). Bosch A; Wiemann S; Guimerà J; Ansorge W; Patterson D; Estivill X Hum Mol Genet; 1993 Oct; 2(10):1744. PubMed ID: 8268937 [No Abstract] [Full Text] [Related]
31. Dinucleotide repeat polymorphisms at the GSR gene. Yu CE; Anderson L; Oshima J; Schellenberg GD Hum Mol Genet; 1994 Jan; 3(1):212. PubMed ID: 8162038 [No Abstract] [Full Text] [Related]
32. Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3. Michelini S; Urbanek M; Dean M; Goldman D Am J Med Genet; 1995 Jun; 60(3):183-7. PubMed ID: 7573168 [TBL] [Abstract][Full Text] [Related]
34. Dinucleotide repeat polymorphism at the D18S365 locus. Abels S; Erdmann J; Nöthen MM Hum Mol Genet; 1993 Oct; 2(10):1747. PubMed ID: 8268941 [No Abstract] [Full Text] [Related]
35. Dinucleotide repeat polymorphism at the D22S351 locus. Sainz J; Rasmussen M; Nechiporuk A; Vissing H; Cheng X; Korenberg JR; Pulst SM Hum Mol Genet; 1993 Oct; 2(10):1749. PubMed ID: 8268946 [No Abstract] [Full Text] [Related]
36. Dinucleotide repeat polymorphism at the D14S294 locus. Fu CW; Anderson L; Schellenberg G Hum Mol Genet; 1993 Oct; 2(10):1751. PubMed ID: 8268948 [No Abstract] [Full Text] [Related]
37. Dinucleotide repeat polymorphism at the D12S371 locus. Leutner A; Schönling J; Spurr NK; Wirth B Hum Mol Genet; 1993 Oct; 2(10):1754. PubMed ID: 8268954 [No Abstract] [Full Text] [Related]
38. Dinucleotide repeat polymorphism at the human GLUT2 locus. Patel P; Lo YM; Bell GI; Turner RC; Wainscoat JS Nucleic Acids Res; 1991 Jul; 19(14):4017. PubMed ID: 1862003 [No Abstract] [Full Text] [Related]
39. Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci. Talbot CC; Warren AC; Avramopoulos D; Antonarakis SE Hum Mol Genet; 1993 Aug; 2(8):1325. PubMed ID: 8401519 [No Abstract] [Full Text] [Related]
40. von Hippel-Lindau syndrome: cloning and identification of the plasma membrane Ca(++)-transporting ATPase isoform 2 gene that resides in the von Hippel-Lindau gene region. Latif F; Duh FM; Gnarra J; Tory K; Kuzmin I; Yao M; Stackhouse T; Modi W; Geil L; Schmidt L Cancer Res; 1993 Feb; 53(4):861-7. PubMed ID: 8428366 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]