Published in Genes Chromosomes Cancer on March 01, 1997
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A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation. J Med Genet (1992) 1.18
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Impaired recognition of disgust in Huntington's disease gene carriers. Brain (1997) 1.13
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Novel ERBB4 juxtamembrane splice variants are frequently expressed in childhood medulloblastoma. Genes Chromosomes Cancer (2001) 1.10
Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes. Blood (1994) 1.10
Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification. Int J Cancer (2001) 1.10
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Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/disseminated neuroblastoma (a SIOPEN collaborative study). Br J Cancer (2011) 1.09
Potential role for concurrent abnormalities of the cyclin D1, p16CDKN2 and p15CDKN2B genes in certain B cell non-Hodgkin's lymphomas. Functional studies in a cell line (Granta 519). Leukemia (1997) 1.09
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The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland. Hum Genet (1990) 1.07
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A polycyclic terpenoid that alleviates oxidative stress. Proc Natl Acad Sci U S A (2008) 1.05
Genomic profile of chronic myelogenous leukemia: Imbalances associated with disease progression. Genes Chromosomes Cancer (2007) 1.04
Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS). Neuroreport (1998) 1.02
A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy. J Biol Chem (2000) 1.01
A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21. Am J Hum Genet (1993) 1.00
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Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. J Med Genet (1996) 0.98
Gain of chromosome arm 17q predicts unfavourable outcome in neuroblastoma patients. U.K. Children's Cancer Study Group and the U.K. Cancer Cytogenetics Group. Eur J Cancer (1997) 0.98
Gain of 1q is a marker of poor prognosis in Wilms' tumors. Genes Chromosomes Cancer (2013) 0.97
A systematic review of oral health assessment by nurses and carers for residents with dementia in residential care facilities. Spec Care Dentist (2006) 0.96
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups. J Med Genet (1993) 0.96
Deletions and rearrangement of CDKN2 in lymphoid malignancy. Blood (1995) 0.96
Erythroleukaemia in the north of England: a population based study. J Clin Pathol (2001) 0.95
Antibiotic resistance: location, location, location. Clin Microbiol Infect (2007) 0.95
Hernia of the lung: a case report and review of literature. Conn Med (1997) 0.94
Comprehensive genetic and histopathologic study reveals three types of neuroblastoma tumors. J Clin Oncol (2001) 0.94
Chromosome translocation in extraskeletal Ewing's tumour. Lancet (1984) 0.94
Flow cytometric enumeration of micronucleated reticulocytes: high transferability among 14 laboratories. Environ Mol Mutagen (2001) 0.94
Assessment of the behaviour and welfare of laying hens on free-range units. Vet Rec (2007) 0.92