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The needle found!!! Trinucleotide repeat expansion in the Hutington's disease geneWILLARD, H. F.Human molecular genetics (Print). 1993, Vol 2, Num 5, pp 497-498, issn 0964-6906Article

Cloning of the X-linked glycerol kinase geneWILLARD, H. F.Human molecular genetics (Print). 1993, Vol 2, Num 2, pp 95-96, issn 0964-6906Article

Chromosome-specific organization of human alpha satellite DNAWILLARD, H. F.American journal of human genetics. 1985, Vol 37, Num 3, pp 524-532, issn 0002-9297Article

The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chainWILLARD, H. F.Human molecular genetics (Print). 1993, Vol 2, Num 10, pp 1525-1526, issn 0964-6906Article

Centromeres: primary constrictions are primarily complicatedWILLARD, H. F.Human molecular genetics (Print). 1992, Vol 1, Num 9, pp 667-668, issn 0964-6906Article

X chromosome inactivation and X-linked mental retardationWILLARD, H. F.American journal of medical genetics. 1996, Vol 64, Num 1, pp 21-26, issn 0148-7299Article

Long-range organization of tandem arrays of α satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stabilityWEVRICK, R; WILLARD, H. F.Proceedings of the National Academy of Sciences of the United States of America. 1989, Vol 86, Num 23, pp 9394-9398, issn 0027-8424Article

Organization, polymorphism, and molecular cytogenetics of chromosome-specific α-satellite DNA from the centromere of chromosome 2HAAF, T; WILLARD, H. F.Genomics (San Diego, Calif.). 1992, Vol 13, Num 1, pp 122-128, issn 0888-7543Article

An assay for X inactivation based on differential methylation at the fragile X locus, FMR1CARREL, L; WILLARD, H. F.American journal of medical genetics. 1996, Vol 64, Num 1, pp 27-30, issn 0148-7299Article

Physical map of the centromeric region of human chromosome 7 : relationship between two distinct alpha satellite arraysWEVRICK, R; WILLARD, H. F.Nucleic acids research. 1991, Vol 19, Num 9, pp 2295-2301, issn 0305-1048, 7 p.Article

A novel transmembrane transporter encoded by the XPCT gene in Xq13.2LAFRENIERE, R. G; CARREL, L; WILLARD, H. F et al.Human molecular genetics (Print). 1994, Vol 3, Num 7, pp 1133-1139, issn 0964-6906Article

The human X-inactivation centre is not required for maintenance of X-chromosome inactivationBROWN, C. J; WILLARD, H. F.Nature (London). 1994, Vol 368, Num 6467, pp 154-156, issn 0028-0836Article

The human aminopeptidase N gene : isolation, chromosome localization, and DNA polymorphism analysisWATT, V. M; WILLARD, H. F.Human genetics. 1990, Vol 85, Num 6, pp 651-654, issn 0340-6717, 4 p.Article

Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixationWAYE, J. S; WILLARD, H. F.Nucleic acids research. 1986, Vol 14, Num 17, pp 6915-6927, issn 0305-1048Article

A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybridsWILLARD, H. F; HOLMES, M. T.Human genetics. 1984, Vol 66, Num 2-3, pp 272-275, issn 0340-6717Article

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx geneCARREL, L; HUNT, P. A; WILLARD, H. F et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1361-1366, issn 0964-6906Article

The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3TRAN-PATERSON, R; WILLARD, H. F; LETARTE, M et al.Cancer genetics and cytogenetics. 1989, Vol 42, Num 1, pp 129-134, issn 0165-4608Article

Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeatWILLARD, H. F; WAYE, J. S.Journal of molecular evolution. 1987, Vol 25, Num 3, pp 207-214, issn 0022-2844Article

Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosomeDURFY, S. J; WILLARD, H. F.American journal of human genetics. 1987, Vol 41, Num 3, pp 391-401, issn 0002-9297Article

Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosomeWAYE, J. S; WILLARD, H. F.Molecular and cellular biology (Print). 1986, Vol 6, Num 9, pp 3156-3165, issn 0270-7306Article

Epigenetic regulation of gene expression : the effect of altered chromatin structure from yeast to mammalsHENDRICH, B. D; WILLARD, H. F.Human molecular genetics (Print). 1995, Vol 4, pp 1765-1777, issn 0964-6906, REVIEWArticle

Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin geneFUJII, J; WILLARD, H. F; MACLENNAN, D. H et al.Somatic cell and molecular genetics. 1990, Vol 16, Num 2, pp 185-189, issn 0740-7750, 5 p.Article

Concerted evolution of primate alpha satellite DNA : evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satelliteDURFY, S. J; WILLARD, H. F.Journal of molecular biology. 1990, Vol 216, Num 3, pp 555-566, issn 0022-2836, 12 p.Article

Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosomeWAYE, J. S; WILLARD, H. F.Molecular and cellular biology (Print). 1986, Vol 6, Num 9, pp 3156-3165, issn 0270-7306Article

Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disordersWILLARD, H. F; RIORDAN, J. R.Science (Washington, D.C.). 1985, Vol 230, Num 4728, pp 940-942, issn 0036-8075Article

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