Published in Hum Genet on August 01, 1996
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The human gene for alkaptonuria (AKU) maps to chromosome 3q. Genomics (1994) 1.99
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Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation. Humangenetik (1971) 1.48
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Two classes of inhibitors of peptidyl transferase activity in eukaryotes. Nature (1974) 1.38
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Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner's syndrome skin fibroblasts. Cytogenet Cell Genet (1981) 1.08
Inhibitors of macromolecular synthesis in yeast. Methods Cell Biol (1975) 1.08
Chromosome banding and DNA replication patterns in bird karyotypes. Cytogenet Cell Genet (1989) 1.07
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Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Nat Genet (1993) 1.07
Utility and limitations of chromosome banding in pre- and postnatal service cytogenetics. Am J Med Genet (1980) 1.05
Second report on chicken genes and chromosomes 2005. Cytogenet Genome Res (2005) 1.05
The relation between well-being, impostor feelings, and gender role orientation among Canadian university students. J Soc Psychol (2001) 1.05
BrdU-Hoechst flow cytometry: a unique tool for quantitative cell cycle analysis. Exp Cell Res (1988) 1.05
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen. Am J Hum Genet (1988) 1.03
Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells. Am J Hum Genet (1985) 1.01
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. J Med Genet (1996) 1.01
Regulation of the integration-excision reaction by bacteriophage lambda. Cold Spring Harb Symp Quant Biol (1981) 1.01
Sources of variation in patient response to radiation treatment. Int J Radiat Oncol Biol Phys (2001) 0.99
A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees. Hum Mol Genet (1997) 0.99
Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay. Lab Invest (2001) 0.99
Functional implications of differential chromosome banding. Am J Hum Genet (1975) 0.98
Cultivated cells from diagnostic amniocentesis in second trimester pregnancies. III. The fetal urine as a potential source of clonable cells. Humangenetik (1975) 0.97
Measuring neuropsychological change following breast cancer treatment: an analysis of statistical models. J Clin Exp Neuropsychol (2008) 0.97
Location of sites in human lipocortin I that are phosphorylated by protein tyrosine kinases and protein kinases A and C. Biochemistry (1988) 0.97
alpha-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorder. J Inherit Metab Dis (1988) 0.97
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation. Am J Hum Genet (1998) 0.96
Morphological and biochemical heterogeneity of amniotic fluid cells in culture. Methods Cell Biol (1982) 0.96
Effects of cytochalasin B on cultivated human diploid fibroblasts and its use for the isolation of tetraploid clones. Exp Cell Res (1973) 0.96
Cellular aging in Werner's syndrome: a unique phenotype? J Invest Dermatol (1979) 0.95
Spectral karyotyping of Werner syndrome fibroblast cultures. Cytogenet Cell Genet (2000) 0.95
Diploid-triploid mixoploidy: clinical and cytogenetic aspects. Pediatrics (1981) 0.94
Disruption of the FA/BRCA pathway in bladder cancer. Cytogenet Genome Res (2007) 0.94
Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35). Ann Genet (1978) 0.94
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. Eur J Hum Genet (2000) 0.93
Methylation of proteins in 60S ribosomal subunits from Saccharomyces cerevisiae. FEBS Lett (1977) 0.93
A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones. Hum Genet (1993) 0.91
Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome. Ann Genet (1971) 0.90
Amniotic fluid cell mosaicism for presumptive trisomy 20. Clin Genet (1978) 0.90
G2 phase cell cycle disturbance as a manifestation of genetic cell damage. Hum Genet (1993) 0.89
Isolation and structural characterization of sialic-acid-containing glycopeptides of the O-glycosidic type from the urine of two patients with an hereditary deficiency in alpha-N-acetylgalactosaminidase activity. Biol Chem Hoppe Seyler (1989) 0.89
Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects. Int J Radiat Oncol Biol Phys (1999) 0.89
Fanconi anemia: causes and consequences of genetic instability. Genome Dyn (2006) 0.89
Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia. Hum Mutat (1998) 0.87
Induction of replicative senescence by 5-azacytidine: fundamental cell kinetic differences between human diploid fibroblasts and NIH-3T3 cells. Cell Prolif (1993) 0.86
Expression analysis and functional activity of interleukin-7 splice variants. Genes Immun (2008) 0.86
Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita. Clin Genet (1992) 0.85
Prenatal genetic diagnosis and elective abortion in women over 35: utilization and relative impact on the birth prevalence of Down syndrome in Washington State. Am J Med Genet (1980) 0.85
Mosaicism in amniotic fluid cell cultures: classification and significance. Am J Med Genet (1978) 0.85
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia. Mol Syndromol (2012) 0.85
Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system. Blood (2000) 0.85
Increased incidence of pulmonary tuberculosis in chronic interstitial lung disease. Thorax (1989) 0.84
Disturbance of cell proliferation by two model compounds of lipid peroxidation contradicts causative role in proliferative senescence. J Cell Physiol (1988) 0.84
Cell-cycle analysis using continuous bromodeoxyuridine labeling and Hoechst 33358-ethidium bromide bivariate flow cytometry. Methods Cell Biol (1994) 0.84
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes. Eur J Pediatr (1992) 0.84