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Markers that discriminate between European and African ancestry show limited variation within Africa.
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- Human Genetics, 2002, v. 111, n. 6, p. 566, doi. 10.1007/s00439-002-0818-z
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- Article
Method for constructing confidently ordered linkage maps.
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- Genetic Epidemiology, 1999, v. 16, n. 4, p. 337, doi. 10.1002/(SICI)1098-2272(1999)16:4<337::AID-GEPI1>3.0.CO;2-T
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- Article
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits.
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- Human Molecular Genetics, 2007, v. 16, n. 2, p. 233, doi. 10.1093/hmg/ddl473
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- Article
STRP Screening Sets for the human genome at 5 cM density.
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- BMC Genomics, 2003, v. 4, p. 6, doi. 10.1186/1471-2164-4-6
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- Article
Barrett's oesophagus: Microsatellite analysis provides evidence to support the proposed metaplasia-dysplasia-carcinoma sequence.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 49, doi. 10.1002/(SICI)1098-2264(199801)21:1<49::AID-GCC7>3.0.CO;2-8
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- Article
Linkage analysis in familial melanoma kindreds to markers on chromosome 6p.
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- International Journal of Cancer, 1994, v. 59, n. 6, p. 771, doi. 10.1002/ijc.2910590611
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- Article
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects.
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- European Journal of Human Genetics, 2009, v. 17, n. 2, p. 258, doi. 10.1038/ejhg.2008.152
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- Article
Quantifying the increase in average human heterozygosity due to urbanisation.
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- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1097, doi. 10.1038/ejhg.2008.48
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- Article
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
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- European Journal of Human Genetics, 2000, v. 8, n. 11, p. 875, doi. 10.1038/sj.ejhg.5200549
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- Article
The Genetic Structure of Pacific Islanders.
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- PLoS Genetics, 2008, v. 4, n. 1, p. e19, doi. 10.1371/journal.pgen.0040019
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- Article
Low Levels of Genetic Divergence across Geographically and Linguistically Diverse Populations from India.
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- PLoS Genetics, 2006, v. 3, n. 6, p. 2052, doi. 10.1371/journal.pgen.0020215
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- Article
Polymorphism near the rat prolactin gene caused by insertion of an Alu-like element.
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- Nature, 1983, v. 305, n. 5930, p. 159, doi. 10.1038/305159a0
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- Article
FIRST CASE OF A NONALLELIC INTERACTION PRODUCT AS A SPECIES-SPECIFIC RED CELL ANTIGEN.
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- Genetics, 1969, v. 62, n. 3, p. 619
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- Article
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis.
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- Pediatric Nephrology, 2003, v. 18, n. 2, p. 105, doi. 10.1007/s00467-002-1018-8
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- Article
Clinical applications of Genome Polymorphism Scans.
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- Biology Direct, 2006, v. 1, p. 16, doi. 10.1186/1745-6150-1-16
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- Article
Mutant deoxynucleotide carrier is associated with congenital microcephaly.
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- Nature Genetics, 2002, v. 32, n. 1, p. 175, doi. 10.1038/ng948
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- Article
The Iceland map.
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- Nature Genetics, 2002, v. 31, n. 3, p. 225, doi. 10.1038/ng920
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- Article
A novel locus for adolescent idiopathic scoliosis on chromosome 12p.
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- Journal of Orthopaedic Research, 2009, v. 27, n. 10, p. 1366, doi. 10.1002/jor.20885
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Comparison of human genetic and sequence-based physical maps.
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- Nature, 2001, v. 409, n. 6822, p. 951, doi. 10.1038/35057185
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Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders.
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- Human Mutation, 2006, v. 27, n. 2, p. 133, doi. 10.1002/humu.20302
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Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.
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- Clinical Genetics, 1995, v. 47, n. 3, p. 122, doi. 10.1111/j.1399-0004.1995.tb03943.x
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- Article
Quantitative Trait Locus Analysis of Atherosclerosis in an Intercross Between C57BL/6 and C3H Mice Carrying the Mutant Apolipoprotein E Gene.
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- Genetics, 2006, v. 172, n. 3, p. 1799, doi. 10.1534/genetics.105.051912
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- Article
Genetic and physical mapping of the McKusick-Kaufman syndrome.
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- Human Molecular Genetics, 1998, v. 7, n. 3, p. 475, doi. 10.1093/hmg/7.3.475
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- Article
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.
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- Human Molecular Genetics, 1998, v. 7, n. 1, p. 63, doi. 10.1093/hmg/7.1.63
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A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps.
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- Human Molecular Genetics, 1995, v. 4, n. 10, p. 1837
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Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers.
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- Human Molecular Genetics, 1995, v. 4, n. 10, p. 1829
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A gene responsible for cavernous malformations of the brain maps to chromosome 7q.
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- Human Molecular Genetics, 1995, v. 4, n. 3, p. 453
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Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome.
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- Human Molecular Genetics, 1995, v. 4, n. 3, p. 449
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Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15.
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- Human Molecular Genetics, 1995, v. 4, n. 3, p. 479
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Genetic linkage of familial expansile osteolysis to chromosome 18q.
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- Human Molecular Genetics, 1994, v. 3, n. 2, p. 359
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Four dinucleotide repeat polymorphisms at the D7S804 locus.
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- Human Molecular Genetics, 1993, v. 2, n. 12, p. 2195
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Mutation of human short tandem repeats.
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- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1123
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Assignment of a gene locus involved in craniosynostosis to chromosome 5qter.
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- Human Molecular Genetics, 1993, v. 2, n. 2, p. 119
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Dinucleotide repeat polymorphisms at the D10S183 and D10S245 loci.
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- Human Molecular Genetics, 1992, v. 1, n. 9, p. 777
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