Transmission ratio distortion in females on chromosome 10p11‐p15
暂无分享,去创建一个
[1] T. Niu,et al. An extreme-sib-pair genome scan for genes regulating blood pressure. , 1999, American journal of human genetics.
[2] A. Paterson,et al. Sex of affected sibpairs and genetic linkage to type 1 diabetes. , 1999, American journal of medical genetics.
[3] L. Cardon,et al. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. , 1999, American journal of human genetics.
[4] K. Clément,et al. A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 , 1998, Nature Genetics.
[5] J C Murray,et al. Pediatrics and , 1998 .
[6] T. Matise,et al. Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium. , 1998, American journal of medical genetics.
[7] R. Straub,et al. A schizophrenia locus may be located in region 10p15-p11. , 1998, American journal of medical genetics.
[8] M. Rietschel,et al. Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis. , 1998, American journal of medical genetics.
[9] Amanda J. Wilson,et al. A search for type 1 diabetes susceptibility genes in families from the United Kingdom , 1998, Nature Genetics.
[10] G. Zubenko,et al. A genome survey for novel Alzheimer disease risk loci: results at 10-cM resolution. , 1998, Genomics.
[11] M. Leppert,et al. Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. , 1998, American journal of human genetics.
[12] J. Rice,et al. Genome-wide search for genes affecting the risk for alcohol dependence. , 1998, American journal of medical genetics.
[13] N. Morton,et al. FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[14] M. Passos-Bueno,et al. Segregation distortion of the CTG repeats at the myotonic dystrophy (DM) locus: new data from Brazilian DM families. , 1997, Journal of medical genetics.
[15] S. Tsuji,et al. Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJD1): evidence for non-Mendelian transmission of the MJD1 gene and for the effect of the intragenic CGG/GGG polymorphism on the intergenerational instability. , 1997, Human molecular genetics.
[16] J. Todd,et al. Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11. , 1997, Human molecular genetics.
[17] F. McMahon,et al. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12. , 1997, American journal of medical genetics.
[18] D. Rubinsztein,et al. Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats. , 1997, Journal of medical genetics.
[19] C. Caskey,et al. Hypermutable myotonic dystrophy CTG repeats in transgenic mice , 1997, Nature Genetics.
[20] L. Schöls,et al. Transmission distortion of the mutant alleles in spinocerebellar ataxia , 1997, Human Genetics.
[21] N. Morton,et al. A metric map of humans: 23,500 loci in 850 bands. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[22] M. McPeek,et al. Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus. , 1996, American journal of human genetics.
[23] M. Shriver,et al. Segregation distortion of the CTG repeats at the myotonic dystrophy locus. , 1996, American journal of human genetics.
[24] A. Fleming. Maternal segregation distortion in sickle-cell trait , 1996, The Lancet.
[25] L Kruglyak,et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.
[26] S. Tsuji,et al. Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis. , 1996, American journal of human genetics.
[27] J. Todd,et al. A genome-wide search for human type 1 diabetes susceptibility genes , 1994, Nature.
[28] Jurg Ott,et al. Handbook of Human Genetic Linkage , 1994 .
[29] C. Valenzuela,et al. Rh segregation distortion: a true reproductive distortion. , 1993, American journal of human genetics.
[30] T. W. Lyttle. Cheaters sometimes prosper: distortion of mendelian segregation by meiotic drive. , 1993, Trends in genetics : TIG.
[31] H. Cann,et al. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. , 1990, Genomics.
[32] E. Lander,et al. Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[33] Eric S. Lander,et al. Faster Multipoint Linkage Analysis Using Fourier Transforms , 1998, J. Comput. Biol..