Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Huntington F. Willard

Veröffentlichungen von Huntington F. Willard zu Willard, Huntington F. ->
weitere Veröffentlichungen von Huntington F. Willard:
Human artificial chromosomes coming into focus (1998)
Genome biology: Tales of the Y chromosome (2003)
Honest Jim talks manners (2007)
Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes (1977)
Counting on Xist (1998)
The genome for the masses (2005)
X-inactivation profile reveals extensive variability in X-linked gene expression in females (2005)
Chromosome-specific α-satellite DNA from the centromere of chimpanzee chromosome 4 (1997)
Orangutan α-satellite monomers are closely related to the human consensus sequence (1998)
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation (1994)
Remodelling chromatin with RNA (1997)
Stable dicentric X chromosomes with two functional centromeres (1998)
Breaking the silence in Rett syndrome (1999)
Human genomics: In search of normality (2006)
Chromosome-specific subsets of human alpha satellite DNA: Analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat (1987)
Veröffentlichungen zu Willard, Huntington F. von Willard, Huntington F.[x]
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
41
Greer, Wenda L., Mahtani, Melanie M., ... Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction
in: Human genetics , ISSN 1432-1203, Vol. 83 (3. 1989), p. 227-230
Zugang: zum Volltext
ähnliche Vorschläge
1989
zeige Details
42
Borsani, Giuseppe, Tonlorenzi, Rossana, ... Characterization of a murine gene expressed from the inactive X chromosome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 351, No. 6324 (1991), p. 325-329
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
43
Brown, Carolyn J., Lafreniere, Ronald G., ... Localization of the X inactivation centre on the human X chromosome in Xq13
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 349, No. 6304 (1991), p. 82-84
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
44
Plenge, Robert M., Hendrich, Brian D., ... A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 17, No. 3 (1997), p. 353-356
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
45
Wolff, D. J., Gustashaw, Karen M., ... Deletions in Xq26.3–q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern
in: Human genetics , ISSN 1432-1203, Vol. 100 (2. 1997), p. 256-262
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
46
Franco, Brunella, Guioli, Silvana, ... A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 353, No. 6344 (1991), p. 529-536
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
47
Ross, Mark T., Grafham, Darren V., ... The DNA sequence of the human X chromosome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 434, No. 7031 (2005), p. 325-337
Zugang: zum Volltext
ähnliche Vorschläge
2005