Published in Chromosome Res on January 01, 2000
A meiotic linkage map of the silver fox, aligned and compared to the canine genome. Genome Res (2007) 1.85
Cross-species chromosome painting unveils cytogenetic signatures for the Eulipotyphla and evidence for the polyphyly of Insectivora. Chromosome Res (2006) 1.49
Reciprocal chromosome painting illuminates the history of genome evolution of the domestic cat, dog and human. Chromosome Res (2000) 1.10
A comparative chromosome map of the Arctic fox, red fox and dog defined by chromosome painting and high resolution G-banding. Chromosome Res (2000) 1.05
Sequence comparison of prefrontal cortical brain transcriptome from a tame and an aggressive silver fox (Vulpes vulpes). BMC Genomics (2011) 0.87
Genotyping-By-Sequencing (GBS) Detects Genetic Structure and Confirms Behavioral QTL in Tame and Aggressive Foxes (Vulpes vulpes). PLoS One (2015) 0.81
Comparative chromosome painting defines the karyotypic relationships among the domestic dog, Chinese raccoon dog and Japanese raccoon dog. Chromosome Res (2003) 0.78
Chromosomal mapping of canine-derived BAC clones to the red fox and American mink genomes. J Hered (2009) 0.77
A second-generation genetic linkage map of the domestic dog, Canis familiaris. Genetics (1999) 1.85
A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps. Genomics (1999) 1.79
A linkage map of the canine genome. Genomics (1997) 1.56
A whole-genome radiation hybrid map of the dog genome. Genomics (1998) 1.32
Molecular evolution of the dog family. Trends Genet (1993) 1.18
The DAPI banded karyotype of the domestic dog (Canis familiaris) generated using chromosome-specific paint probes. Chromosome Res (1999) 1.16
Chromosome-specific paints from a high-resolution flow karyotype of the dog. Chromosome Res (1996) 1.04
Gene localization and syntenic mapping by FISH in the dog. Cytogenet Cell Genet (1996) 0.99
Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5. Genomics (1997) 0.94
Towards construction of a canine linkage map: establishment of 16 linkage groups. Mamm Genome (1997) 0.92
Report on the progress of standardization of the G-banded canine (Canis familiaris) karyotype. Committee for the Standardized Karyotype of the Dog (Canis familiaris). Chromosome Res (1996) 0.91
The Giemsa banding pattern of the canine karyotype. Cytogenet Cell Genet (1975) 0.91
An extended nomenclature of the canine karyotype. Cytogenet Cell Genet (1996) 0.87
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency. Genomics (1994) 0.81
High-resolution GTG-banding patterns of dog and silver fox chromosomes: description and comparative analysis. Cytogenet Cell Genet (1995) 0.81
The standard karyotype of the silver for (Vulpes fulvus Desm.). Committee for the standard karyotype of Vulpes fulvus Desm. Hereditas (1985) 0.80
The highly polymorphic canine microsatellite ZuBeCa6 is localized on canine chromosome 5q12-q13. Anim Genet (1998) 0.80
The application of FISH techniques for physical mapping in the dog (Canis familiaris). Mamm Genome (1996) 0.78
Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization. Mamm Genome (1996) 0.77
The highly polymorphic canine microsatellite ZuBeCa4 is localized on canine chromosome 3q15-q18. Anim Genet (1998) 0.75
Assignment of the canine microsatellite CanBern6 to the canine chromosome group 22 to 38. Anim Genet (1997) 0.75
Twelve novel cosmid-derived canine microsatellites. Anim Genet (1999) 0.75
Assignment of the canine microsatellite CanBern1 to canine chromosome 13q21. Anim Genet (1997) 0.75
The highly polymorphic canine microsatellite ZuBeCa2 is localized on canine chromosome 1q210-q211. Anim Genet (1998) 0.75
Assignment of the canine microsatellite ZuBeCa3 to canine chromosome 9q21-q22. Anim Genet (1998) 0.75
Assignment of the canine microsatellite ZuBeCa5 to canine chromosome 19q7. Anim Genet (1998) 0.75
Assignment of the canine microsatellite ZuBeCa1 to canine chromosome 10q22-q24. Anim Genet (1998) 0.75
Multicolor spectral karyotyping of human chromosomes. Science (1996) 7.65
Microsatellite evolution--evidence for directionality and variation in rate between species. Nat Genet (1995) 4.77
Clinical features and natural history of von Hippel-Lindau disease. Q J Med (1990) 4.71
Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion. J Med Genet (1971) 4.70
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13
Von Hippel-Lindau disease: a genetic study. J Med Genet (1991) 3.61
Translocation of c-ab1 oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia. Nature (1984) 3.24
Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction. Nucleic Acids Res (1985) 3.09
Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization. Proc Natl Acad Sci U S A (1982) 3.07
Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes. Genes Chromosomes Cancer (1992) 3.03
A possible novel interaction between the 3'-end of 18 S ribosomal RNA and the 5'-leader sequence of many eukaryotic messenger RNAs. FEBS Lett (1982) 2.91
Multicolour spectral karyotyping of mouse chromosomes. Nat Genet (1996) 2.90
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat (1996) 2.80
X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome. Lancet (1966) 2.68
Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma. Hum Mol Genet (1994) 2.65
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. Hum Mol Genet (1994) 2.52
Oncogenicity of non-transforming mutants of avian sarcoma viruses. J Gen Virol (1973) 2.14
Stereoselective block of hERG channel by (S)-methadone and QT interval prolongation in CYP2B6 slow metabolizers. Clin Pharmacol Ther (2007) 2.06
Rapid determination of sequences flanking microsatellites. Nucleic Acids Res (1991) 2.04
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. Genomics (1988) 2.04
Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses. Prenat Diagn (1984) 1.97
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome. Nature (1983) 1.94
Human centromeric DNAs. Hum Genet (1997) 1.94
Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes. Nat Genet (1993) 1.92
Avoidance of anencephalic and spina bifida births by maternal serum-alphafetoprotein screening. Lancet (1978) 1.90
The reduction of anencephalic and spina bifida births by maternal serum alphafetoprotein screening. Br Med Bull (1983) 1.89
Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. J Med Genet (1992) 1.85
A comparative study of karyotypes of muntjacs by chromosome painting. Chromosoma (1995) 1.81
A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps. Genomics (1999) 1.79
Reciprocal chromosome painting among human, aardvark, and elephant (superorder Afrotheria) reveals the likely eutherian ancestral karyotype. Proc Natl Acad Sci U S A (2003) 1.79
A whole-genome radiation hybrid panel for bovine gene mapping. Mamm Genome (1997) 1.77
Gender verification in the Olympics. JAMA (2000) 1.72
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence. Nat Genet (1994) 1.71
High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry. Proc Natl Acad Sci U S A (1981) 1.65
Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34. Hum Genet (1976) 1.63
Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency). Nucleic Acids Res (1987) 1.62
CA repeat polymorphism at the ASS locus. Nucleic Acids Res (1990) 1.59
Letter: Prospective data on risk of Down syndrome in relation to maternal age. Lancet (1976) 1.57
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number. Hum Mol Genet (1993) 1.56
Chromosomal localization of a single copy gene by in situ hybridization--human beta globin genes on the short arm of chromosome 11. Ann Hum Genet (1981) 1.56
Comparative genomics: tracking chromosome evolution in the family ursidae using reciprocal chromosome painting. Cytogenet Cell Genet (1998) 1.54
Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2. Nat New Biol (1973) 1.49
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7. Cytogenet Cell Genet (1978) 1.48
Disruption of the neuronal PAS3 gene in a family affected with schizophrenia. J Med Genet (2003) 1.46
Prenatal assessment of anterior abdominal wall defects and their prognosis. Prenat Diagn (1985) 1.45
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Proc Natl Acad Sci U S A (1989) 1.43
Determination of the DNA content of human chromosomes by flow cytometry. Cytogenet Cell Genet (1986) 1.40
Variable transfer of Y-specific sequences in XX males. Nucleic Acids Res (1986) 1.40
Sanfilippo A disease in the fetus. J Med Genet (1974) 1.40
Which prenatal screening protocol? Prenat Diagn (2004) 1.39
Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects? Clin Genet (1987) 1.35
Chromosome analysis before birth and its value in genetic counselling. Br Med J (1971) 1.35
cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog. Invest Ophthalmol Vis Sci (1999) 1.28
Localization of the human alpha-globin gene cluster to the short arm of chromosome 16 (16p12-16pter) by hybridization in situ. J Mol Biol (1982) 1.27
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programme. Prenat Diagn (1994) 1.26
Prenatal chromosome analysis and its impact on the birth incidence of chromosome disorders. Br Med Bull (1983) 1.26
Karyotype relationships between four distantly related marsupials revealed by reciprocal chromosome painting. Chromosome Res (1999) 1.25
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene. Hum Mol Genet (1995) 1.25
Predictive value of amniotic acetylcholinesterase analysis in the diagnosis of fetal abnormality in 3700 pregnancies. Prenat Diagn (1985) 1.25
Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl. J Med Genet (1987) 1.24
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics (1989) 1.22
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots. Cytometry (1990) 1.22
Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma. J Med Genet (1990) 1.21
Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes. Nucleic Acids Res (1987) 1.18
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry. Hum Genet (1986) 1.16
Conservation of human vs. feline genome organization revealed by reciprocal chromosome painting. Cytogenet Cell Genet (1997) 1.16
Analysis of pilocytic astrocytoma by comparative genomic hybridization. Br J Cancer (2000) 1.16
Frequency of autoantibodies in patients with chromatin-positive Klinefelter's syndrome and their parents. Lancet (1966) 1.13
Cross-species chromosome painting in the golden mole and elephant-shrew: support for the mammalian clades Afrotheria and Afroinsectiphillia but not Afroinsectivora. Proc Biol Sci (2004) 1.13
Reciprocal chromosome painting between two South American bats: Carollia brevicauda and Phyllostomus hastatus (Phyllostomidae, Chiroptera). Chromosome Res (2005) 1.13
Inherited constriction fragility of chromosome 2. Ann Genet (1973) 1.12
Reciprocal chromosome painting shows that the great difference in diploid number between human and African green monkey is mostly due to non-Robertsonian fissions. Mamm Genome (1999) 1.11
Prenatal diagnosis and family studies in a case of propionicacidaemia. Clin Genet (1975) 1.11
Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet (1998) 1.11
Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry. Nat Genet (1993) 1.10
Reciprocal chromosome painting illuminates the history of genome evolution of the domestic cat, dog and human. Chromosome Res (2000) 1.10
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels. Genomics (1989) 1.09
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis. Genomics (1991) 1.09
Non-homologous sex chromosomes in two species of the genus Eigenmannia (Teleostei: Gymnotiformes). Cytogenet Genome Res (2008) 1.08
Reversal and convergence in marsupial chromosome evolution. Cytogenet Genome Res (2003) 1.08
Conservation of human gamma-X centromeric satellite DNA among primates with an autosomal localization in certain Old World monkeys. Chromosome Res (1999) 1.08
Gender verification of female athletes. Genet Med (2001) 1.07
Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene. J Med Genet (1986) 1.06
Recurrent cardioembolic stroke related to late dislodgement of a right atrial pacing lead into the left atrium. Europace (1999) 1.06
A dinucleotide repeat polymorphism at the D9S127 locus. Nucleic Acids Res (1992) 1.06
Amniotic-fluid alpha-fetoprotein in the antenatal diagnosis of spina bifida. Lancet (1973) 1.06
Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers. Genomics (1987) 1.05
Genetic diversity in Swiss goat breeds based on microsatellite analysis. Anim Genet (1999) 1.05
Reciprocal chromosome painting shows that genomic rearrangement between rat and mouse proceeds ten times faster than between humans and cats. Cytogenet Cell Genet (1999) 1.05
A comparative chromosome map of the Arctic fox, red fox and dog defined by chromosome painting and high resolution G-banding. Chromosome Res (2000) 1.05
The psychosocial sequelae of a second-trimester termination of pregnancy for fetal abnormality. Prenat Diagn (1992) 1.05
Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22. Br J Cancer (1994) 1.04
Complete genomic sequence of the bovine prion gene (PRNP) and polymorphism in its promoter region. Anim Genet (2001) 1.04
Defining the ancestral karyotype of all primates by multidirectional chromosome painting between tree shrews, lemurs and humans. Chromosoma (1999) 1.03
Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi). J Med Genet (1969) 1.03