Published in Am J Hum Genet on July 01, 1985
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Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet (1989) 2.56
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium. Am J Hum Genet (1992) 1.94
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Further linkage data on cystic fibrosis: the Utah Study. Am J Hum Genet (1986) 1.63
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Isolation and regional mapping of DNA sequences unique to human chromosome 21. Am J Hum Genet (1987) 1.30
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. Am J Hum Genet (1987) 1.24
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Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis. Am J Hum Genet (1988) 1.14
Parental origin of de novo constitutional deletions of chromosomal band 11p13. Am J Hum Genet (1990) 1.10
Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene. Nucleic Acids Res (1989) 1.07
Eight closely linked loci place the Wilson disease locus within 13q14-q21. Am J Hum Genet (1988) 1.07
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. Am J Hum Genet (1994) 1.06
Localization of HeLa cell tumor-suppressor gene to the long arm of chromosome II. Am J Hum Genet (1989) 1.00
Ig gamma restriction fragment length polymorphisms indicate an ancient separation of Caucasian haplotypes. Am J Hum Genet (1986) 1.00
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Krabbe disease locus mapped to chromosome 14 by genetic linkage. Am J Hum Genet (1990) 0.97
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Recombinant DNA techniques in the diagnosis of inherited disorders. J Clin Invest (1986) 0.91
High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q. Proc Natl Acad Sci U S A (1988) 0.90
A deletion map of the WAGR region on chromosome 11. Am J Hum Genet (1989) 0.89
RFLP analysis of HLA-DR and -DQ genes and their linkage relationships in the Pacific. Am J Hum Genet (1986) 0.88
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Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer. Am J Hum Genet (1990) 0.75
Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter. Am J Hum Genet (1990) 0.75
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A strategy to reveal high-frequency RFLPs along the human X chromosome. Am J Hum Genet (1984) 7.73
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Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. Proc Natl Acad Sci U S A (1984) 4.22
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13. Am J Hum Genet (1984) 3.86
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Abbreviated regimens of zidovudine prophylaxis and perinatal transmission of the human immunodeficiency virus. N Engl J Med (1998) 5.65
Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol (1998) 5.42
Nuclear DNA polymorphism in a Mandenka population from Senegal: comparison with eight other human populations. Ann Hum Genet (1995) 5.34
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Study of 47 DNA markers in five populations from four continents. Gene Geogr (1987) 4.04
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Demographic history of India and mtDNA-sequence diversity. Am J Hum Genet (1995) 3.47
Severe B cell hyperplasia and autoimmune disease in TALL-1 transgenic mice. Proc Natl Acad Sci U S A (2000) 3.37
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Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. Am J Hum Genet (1986) 3.17
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data. Am J Hum Genet (1986) 3.16
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Mch3, a novel human apoptotic cysteine protease highly related to CPP32. Cancer Res (1995) 2.47
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