Published in Nature on September 06, 1974
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Transcriptional activation of the translocated c-myc oncogene in burkitt lymphoma. Proc Natl Acad Sci U S A (1983) 3.46
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Translocation of immunoglobulin VH genes in Burkitt lymphoma. Proc Natl Acad Sci U S A (1982) 3.30
A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man. Proc Natl Acad Sci U S A (1983) 2.73
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Assignment of the structural gene for the third component of human complement to chromosome 19. Proc Natl Acad Sci U S A (1982) 2.00
Receptors for human alpha and beta interferon but not for gamma interferon are specified by human chromosome 21. Proc Natl Acad Sci U S A (1984) 1.86
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Multiple dispersed loci produce small cytoplasmic Alu RNA. Mol Cell Biol (1993) 1.54
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Introduction of a human X-6 translocation chromosome into a mouse teratocarcinoma: investigation of control of HLA-A, B, C expression. Proc Natl Acad Sci U S A (1982) 1.33
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. Proc Natl Acad Sci U S A (1985) 1.22
Chromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene family. Proc Natl Acad Sci U S A (1985) 1.19
The chromosome 14 breakpoint in neoplastic B cells with the t(11;14) translocation involves the immunoglobulin heavy chain locus. Proc Natl Acad Sci U S A (1984) 1.17
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A human Alu RNA-binding protein whose expression is associated with accumulation of small cytoplasmic Alu RNA. Mol Cell Biol (1994) 1.01
The human Y4 small cytoplasmic RNA gene is controlled by upstream elements and resides on chromosome 7 with all other hY scRNA genes. Nucleic Acids Res (1994) 1.01
Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis. Proc Natl Acad Sci U S A (1982) 1.01
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Integration of Ecogpt and SV40 early region sequences into human chromosome 17: a dominant selection system in whole cell and microcell human-mouse hybrids. EMBO J (1983) 0.99
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Alcohol dehydrogenase mutants of Chinese hamster somatic cells resistant to allyl alcohol. Genetics (1978) 0.82
The conserved 7SK snRNA gene localizes to human chromosome 6 by homolog exclusion probing of somatic cell hybrid RNA. Nucleic Acids Res (1994) 0.81
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Assignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1. Am J Hum Genet (1989) 0.76
Differentiation in vitro of human-mouse teratocarcinoma hybrids. Mol Cell Biol (1983) 0.76
Identification of a cell-surface antigen produced by a gene on human chromosome 3 (cen-q22) and not expressed by Rhnull cells. Am J Hum Genet (1987) 0.76
The E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor. Am J Hum Genet (1985) 0.75
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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature (1993) 7.39
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Technique for identifying Y chromosomes in human interphase nuclei. Nature (1970) 3.64
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A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics (1988) 3.18
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain. J Med Genet (2004) 2.83
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy. Science (1988) 2.82
Amniotic-fluid acetylcholinesterase as a possible diagnostic test for neural-tube defects in early pregnancy. Lancet (1979) 2.42
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nat Genet (1996) 2.32
The new genetics. Implications for clinical services in Britain and the United States. BMJ (1998) 2.30
The beta2-microglobulin gene is on chromosome 15 and not in the HL-A region. Nature (1975) 2.29
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Results of first year (1989) of a national register of Down's syndrome in England and Wales. BMJ (1991) 2.07
Angiostrongylus cantonensis infection from eating raw snails. N Engl J Med (1995) 2.07
Antenatal screening in Oxford for fetal neural tube defects. Br J Obstet Gynaecol (1979) 2.06
The role of Shigella spp., enteroinvasive Escherichia coli, and other enteropathogens as causes of childhood dysentery in Thailand. J Infect Dis (1986) 2.06
Two cases of X/autosome translocation in females with incontinentia pigmenti. Hum Genet (1985) 2.05
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Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9. Nat New Biol (1972) 1.91
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Molecular phylogenetic analysis of Cyclospora, the human intestinal pathogen, suggests that it is closely related to Eimeria species. J Infect Dis (1996) 1.82
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring. J Med Genet (1975) 1.81
Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up. UK Cystic Fibrosis Follow-Up Study Group. Lancet (1996) 1.79
Definitive evidence for the short arm of the Y chromosome associating with the X chromosome during miosis in the human male. Nature (1970) 1.78
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The junctional multidomain protein AF-6 is a binding partner of the Rap1A GTPase and associates with the actin cytoskeletal regulator profilin. Proc Natl Acad Sci U S A (2000) 1.68
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Prenatal detection of unbalanced chromosomal rearrangements by array CGH. J Med Genet (2005) 1.63
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Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. J Med Genet (1996) 1.55
Prenatal testing for Duchenne and Becker muscular dystrophy. Lancet (1988) 1.54
Gambling and pathological gambling among university students. Addict Behav (1991) 1.53
Wegener granulomatosis: MR imaging findings in brain and meninges. Radiology (1999) 1.53
A method for generating hybrids containing nonselected fragments of human chromosomes. Genomics (1989) 1.47
Point mutations in the dystrophin gene. Proc Natl Acad Sci U S A (1992) 1.46
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13. Ann Hum Genet (1975) 1.45
Exon structure of the human dystrophin gene. Genomics (1993) 1.45
Non echo planar, diffusion-weighted magnetic resonance imaging (periodically rotated overlapping parallel lines with enhanced reconstruction sequence) compared with echo planar imaging for the detection of middle-ear cholesteatoma. J Laryngol Otol (2010) 1.45
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Human gene mapping using an X/autosome translocation. Somatic Cell Genet (1976) 1.44
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA. Lancet (1991) 1.44
The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care. Br J Cancer (2007) 1.43
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes. Am J Hum Genet (1991) 1.41
Conventional digital subtraction x-ray angiography versus magnetic resonance angiography in the evaluation of carotid disease: patient satisfaction and preferences. Clin Radiol (2004) 1.40
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Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations. Hum Mutat (1994) 1.36
Effect of purified luteinizing hormone releasing factor on normal and hypogonadotrophic anosmic men. Nature (1971) 1.36
Detection of novel genetic markers by mismatch analysis. Nucleic Acids Res (1989) 1.36
Latex allergy in hospital employees. Ann Allergy (1994) 1.33
Genetic counselling: the psychological impact of meeting patients' expectations. J Med Genet (1997) 1.33
Nondirectiveness in genetic counseling: an empirical study. Am J Hum Genet (1997) 1.32
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene. Genomics (1990) 1.31
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR. Genomics (1991) 1.31
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. J Med Genet (1989) 1.30
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE. Hum Mol Genet (1993) 1.29
Evidence for the assignment of the loci AK1, AK3 and ACONs to chromosome 9 in man. Ann Hum Genet (1976) 1.29
The impact of population based screening for carriers of cystic fibrosis. J Med Genet (1994) 1.27
Numbers or words? A randomized controlled trial of presenting screen negative results to pregnant women. Prenat Diagn (2000) 1.26
Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16. Ann Hum Genet (1980) 1.26
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. J Med Genet (1991) 1.23
Polymicrobial aetiology of travellers' diarrhoea. Lancet (1985) 1.23
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Mixed Candida albicans and Candida glabrata populations associated with the pathogenesis of denture stomatitis. Oral Microbiol Immunol (2008) 1.19
Sister chromatid exchanges--a sensitive assay of agents damaging human chromosomes. Mutat Res (1975) 1.18
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DNA deletions in mild and severe Becker muscular dystrophy. Hum Genet (1987) 1.14
Prenatal diagnosis by array-CGH. Eur J Med Genet (2005) 1.11
Confirmation and further regional assignment of aminoacylase 1 (acy-1) on human chromosome 3 using a simplified detection method. Ann Hum Genet (1980) 1.10
The search for a human equivalent of the mouse T-locus - negative results from a study of HL-A types in spina bifida. Tissue Antigens (1975) 1.10
Structural variation in chromosome No 9. Ann Genet (1974) 1.10
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter. Hum Mol Genet (1994) 1.09
A complex chromosomal rearrangement with formation of a ring 4. J Med Genet (1971) 1.08
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR. Genomics (1992) 1.08
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Localization of the gene for classic Alport syndrome. Genomics (1989) 1.05
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Fetal growth restriction: a workshop report. Placenta (2004) 1.03
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease. J Med Genet (1992) 1.01
The identification of a repeated DNA sequence involved in the karyotype polymorphism of the human Y chromosome. Cytogenet Cell Genet (1978) 1.01
The effects of various banding procedures on human chromosomes, studied with acridine orange. Cytogenet Cell Genet (1973) 1.01
Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes. Cytogenetics (1971) 1.00
The sites of radiation induced-breakage in human lymphocyte chromosomes, determined by quinacrine fluorescence. Mutat Res (1973) 1.00
Dystrophins in vertebrates and invertebrates. Hum Mol Genet (1998) 0.99
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy. J Med Genet (1987) 0.99