Robert Gemmill to Chromosomes, Human, Pair 3
This is a "connection" page, showing publications Robert Gemmill has written about Chromosomes, Human, Pair 3.
Connection Strength
1.711
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Molecular definition of a small amplification domain within 3q26 in tumors of cervix, ovary, and lung. Cancer Genet Cytogenet. 2000 Feb; 117(1):9-18.
Score: 0.165
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Homozygous deletions of human chromosome 3p in lung tumors. Cancer Res. 1997 Apr 01; 57(7):1344-52.
Score: 0.136
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A second-generation YAC contig map of human chromosome 3. Nature. 1995 Sep 28; 377(6547 Suppl):299-319.
Score: 0.122
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YAC contigs covering an 8-megabase region of 3p deleted in the small-cell lung cancer cell line U2020. Genomics. 1995 Jan 01; 25(1):19-28.
Score: 0.116
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Dinucleotide repeat polymorphism (D3S1776) on human chromosome 3p. Hum Mol Genet. 1994 May; 3(5):841.
Score: 0.111
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Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation. Cancer Genet. 2014 Apr; 207(4):133-40.
Score: 0.110
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Characterization of the submicroscopic deletion in the small-cell lung carcinoma (SCLC) cell line U2020. Genes Chromosomes Cancer. 1992 Jul; 5(1):67-74.
Score: 0.097
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Report of the Second International Workshop on Human Chromosome 3 mapping. Cytogenet Cell Genet. 1991; 57(4):162-6.
Score: 0.088
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A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma. Genes Chromosomes Cancer. 2007 Sep; 46(9):805-12.
Score: 0.070
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DEF-3(g16/NY-LU-12), an RNA binding protein from the 3p21.3 homozygous deletion region in SCLC. Oncogene. 1999 Apr 22; 18(16):2589-97.
Score: 0.039
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Chromosomal duplication accompanies allelic loss in non-small cell lung carcinoma. Cancer Res. 1998 Oct 15; 58(20):4701-7.
Score: 0.038
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The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8. Proc Natl Acad Sci U S A. 1998 Aug 04; 95(16):9572-7.
Score: 0.037
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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet. 1997 Sep; 17(1):65-70.
Score: 0.035
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A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia loci. Eur J Hum Genet. 1997 May-Jun; 5(3):171-4.
Score: 0.034
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Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B. Hum Mol Genet. 1997 Feb; 6(2):193-203.
Score: 0.033
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The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. Am J Hum Genet. 1996 Dec; 59(6):1328-36.
Score: 0.033
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Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorin. Oncogene. 1996 Mar 21; 12(6):1289-97.
Score: 0.032
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Report of the sixth international workshop on human chromosome 3 mapping 1995. Cytogenet Cell Genet. 1996; 72(4):255-70.
Score: 0.031
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Assignment of the human slow twitch skeletal muscle/cardiac troponin C gene (TNNC1) to human chromosome 3p21.3-->3p14.3 using somatic cell hybrids. Cytogenet Cell Genet. 1996; 75(1):36-7.
Score: 0.031
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Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma. Genes Chromosomes Cancer. 1995 Mar; 12(3):224-8.
Score: 0.029
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Report and abstracts of the fifth international workshop on human chromosome 3 mapping 1994. Ann Arbor, Michigan, May 8-9, 1994. Cytogenet Cell Genet. 1995; 68(3-4):125-46.
Score: 0.029
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Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B. Genes Chromosomes Cancer. 1994 Dec; 11(4):216-21.
Score: 0.029
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Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats. Chromosome Res. 1994 Nov; 2(6):423-7.
Score: 0.029
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Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL). Cancer Genet Cytogenet. 1994 Oct; 77(1):1-13.
Score: 0.028
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Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics. 1994 Jul 15; 22(2):319-26.
Score: 0.028
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Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies. Cancer Genet Cytogenet. 1993 Nov; 71(1):15-21.
Score: 0.027
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Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint. Proc Natl Acad Sci U S A. 1993 Sep 15; 90(18):8509-13.
Score: 0.027
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A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome. Genomics. 1991 Sep; 11(1):93-102.
Score: 0.023
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Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndrome. Cancer Genet Cytogenet. 1989 Jun; 39(2):289-93.
Score: 0.020
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Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). Genomics. 1989 May; 4(4):518-29.
Score: 0.020
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A 1.5-megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma. Genomics. 1989 Jan; 4(1):28-35.
Score: 0.019
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Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. Cancer Genet Cytogenet. 1988 Mar; 31(1):69-73.
Score: 0.018
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Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14. Cancer Genet Cytogenet. 1988 Mar; 31(1):75-82.
Score: 0.018
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Angiogenic squamous dysplasia in bronchi of individuals at high risk for lung cancer. Clin Cancer Res. 2000 May; 6(5):1616-25.
Score: 0.010