Published in Hum Mol Genet on April 01, 1993
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New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locus. Nucleic Acids Res (2005) 0.85
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Seven polymorphic loci mapping to human chromosomal region 11q22-qter. Genomics (1988) 2.23
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A detailed genetic map of the long arm of chromosome 11. Genomics (1990) 2.11
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Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2. Am J Hum Genet (2000) 1.82
Report of the committee on the genetic constitution of chromosomes 20 and 21. Cytogenet Cell Genet (1989) 1.80
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A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLP. Am J Hum Genet (1990) 1.54
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women. Am J Hum Genet (1996) 1.54
Tetranucleotide repeat polymorphism at the D21S11 locus. Hum Mol Genet (1992) 1.53
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds. Am J Hum Genet (1991) 1.53
Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. Am J Hum Genet (1986) 1.50
Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p. Am J Hum Genet (1991) 1.43
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Detection and characterization of additional DNA polymorphisms in the dopamine D2 receptor gene. Genomics (1991) 1.38
A hypervariable RFLP on chromosome 17p13 is defined by an arbitrary single copy probe p144-D6 [HGM9 No. D17S34]. Nucleic Acids Res (1987) 1.37
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13. Nat Genet (1996) 1.36
Rheology of the vitreous body. Part I: Viscoelasticity of human vitreous. Biorheology (1993) 1.30
Rapid human chromosome aberration analysis using fluorescence in situ hybridization. Int J Radiat Biol (1989) 1.28
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease. J Card Fail (2001) 1.27
Social and psychological theories and their use for dental practice. Int Dent J (1993) 1.20
Kethoxal inactivation of three transfer ribonucleic acids chargeable by yeast phenylalanyl transfer ribonucleic acid synthetase. Biochemistry (1972) 1.16
A hypervariable repeated sequence on human chromosome 1p36. Hum Genet (1987) 1.15
Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11. Am J Hum Genet (1994) 1.14
A new locus for autosomal dominant congenital cataracts maps to chromosome 3. Invest Ophthalmol Vis Sci (2000) 1.14
A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22. Genomics (1996) 1.13
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A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia. Neurology (1999) 1.11
A biopsychosocial model to predict caries in preschool children. Pediatr Dent (1995) 1.09
A simple procedure for the purification of yeast phenylalanine transfer RNA. Biochem Biophys Res Commun (1968) 1.08
Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. Hum Genet (1986) 1.07
High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus. Am J Hum Genet (1992) 1.07
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library. Hum Genet (1986) 1.07
Mucus rheology: relation to structure and function. Biorheology (1976) 1.07
Dinucleotide repeat polymorphism at the PGK1 locus. Nucleic Acids Res (1991) 1.06
Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoforms. Genomics (1994) 1.06
Human cervical mucus. IV. Viscoelasticity and sperm penetrability during the ovulatory menstrual cycle. Fertil Steril (1978) 1.05
Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization. Am J Hum Genet (1983) 1.04
Characterization of (CA)n microsatellites with degenerate sequencing primers. Nucleic Acids Res (1992) 1.03
Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa. Am J Hum Genet (1990) 1.03
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Viscoelasticity of mucus. Its role in ciliary transport of pulmonary secretions. Am Rev Respir Dis (1968) 1.02
TG repeat polymorphism at the D21S167 locus. Nucleic Acids Res (1990) 1.02
Dinucleotide repeat polymorphism at the D14S43 locus. Nucleic Acids Res (1991) 1.00
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Bispectral analysis of visual interactions in humans. Electroencephalogr Clin Neurophysiol (1996) 1.00
A study of mucus glycoproteins in secretory otitis media. Arch Otolaryngol (1985) 1.00
Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease. Lancet (1998) 1.00
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Composition and functioin of human cervical mucus. Biochim Biophys Acta (1980) 0.98
Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. Am J Hum Genet (1986) 0.96
Inactivation of yeast phenylalanine transfer ribonucleic acid by kethoxal. Biochemistry (1971) 0.96
Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q. Genomics (1992) 0.96
Studies of the familial aggregation of chronic bronchitis and obstructive airways disease. Int J Epidemiol (1978) 0.95
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. Am J Hum Genet (1993) 0.95
The viscoelasticity of fractionated canine tracheal mucus. Biorheology (1974) 0.94
Sorsby fundus dystrophy. A family with the Ser181Cys mutation of the tissue inhibitor of metalloproteinases 3. Arch Ophthalmol (1996) 0.94
Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. Hum Mol Genet (1995) 0.93
Dinucleotide repeat polymorphism at the D11S527 locus. Nucleic Acids Res (1991) 0.93
Vancomycin-resistant enterococci on a renal ward in an Ontario hospital. Can Commun Dis Rep (1996) 0.93
Human cervical mucus. II. Changes in viscoelasticity during the ovulatory menstrual cycle. Fertil Steril (1977) 0.92
Human cervical mucus. III. Isolation and characterization of rheologically active mucin. Fertil Steril (1977) 0.92
Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome. Hum Hered (1990) 0.91
Dinucleotide repeat polymorphism at the D14S45 locus. Nucleic Acids Res (1991) 0.90
Dinucleotide repeat polymorphism at the PGK1P1 locus. Nucleic Acids Res (1992) 0.90
Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide. J Neurol Neurosurg Psychiatry (1995) 0.90
A high resolution CEPH crossover mapping panel and integrated map of chromosome 11. Hum Mol Genet (1996) 0.89
Dinucleotide repeat polymorphism at the D11S528 locus. Nucleic Acids Res (1991) 0.89
Dinucleotide repeat polymorphism at the DXYS1X locus. Nucleic Acids Res (1991) 0.88
Population genetics of the highly polymorphic locus D16S7 and its use in paternity evaluation. Am J Hum Genet (1989) 0.88
Human cervical mucus. I. Rheologic characteristics. Fertil Steril (1977) 0.88
The Babington nebulizer: a new principle for generation of therapeutic aerosols. Am Rev Respir Dis (1972) 0.88
Dinucleotide repeat polymorphism at the human chromosome 11p telomere (D11S2071). Genomics (1995) 0.88
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1. Am J Hum Genet (1994) 0.87
Tricarboxylic acid cycle activity in postischemic rat hearts. Circulation (1993) 0.87
Functional aspects of mucus rheology. Adv Exp Med Biol (1977) 0.87
Effect of Ca++ on the structure and rheology of canine tracheal mucin. Biorheology (1984) 0.87
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19. Hum Genet (1986) 0.86
Human cytochrome c oxidase subunit VIb: characterization and mapping of a multigene family. Gene (1991) 0.86
Dinucleotide repeat polymorphism at the D21S13E locus. Nucleic Acids Res (1990) 0.86
Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci. Hum Mol Genet (1992) 0.86
No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology (1995) 0.86
An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]. Nucleic Acids Res (1987) 0.86