The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms.

Por Page, D C, de la Chapelle, A
Publicado em 1984

Expression of DAZ, an azoospermia factor candidate, in human spermatogonia.

Por Menke, D B, Mutter, G L, Page, D C
Publicado em 1997

XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation.

Por Ramsay, M, Bernstein, R, Zwane, E, Page, D C, Jenkins, T
Publicado em 1988

Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome.

Por Tsuchiya, K, Reijo, R, Page, D C, Disteche, C M
Publicado em 1995

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

Por Hassold, T J, Sherman, S L, Pettay, D, Page, D C, Jacobs, P A
Publicado em 1991

A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies.

Por Bernstein, R, Rosendorff, J, Ramsay, M, Pinto, M R, Page, D C
Publicado em 1987

Inactivation of the Zfx gene on the mouse X chromosome.

Por Adler, D A, Bressler, S L, Chapman, V M, Page, D C, Disteche, C M
Publicado em 1991

Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.

Por Zinn, A R, Alagappan, R K, Brown, L G, Wool, I, Page, D C
Publicado em 1994

An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome.

Por Knowlton, R G, Nelson, C A, Brown, V A, Page, D C, Donis-Keller, H
Publicado em 1989

Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers.

Por Mardon, G, Luoh, S W, Simpson, E M, Gill, G, Brown, L G, Page, D C
Publicado em 1990

A 45,X male with Y-specific DNA translocated onto chromosome 15.

Por Gal, A, Weber, B, Neri, G, Serra, A, Müller, U, Schempp, W, Page, D C
Publicado em 1987

The origin of 45,X males.

Por de la Chapelle, A, Page, D C, Brown, L, Kaski, U, Parvinen, T, Tippett, P A
Publicado em 1986

Small deletions of the short arm of the Y chromosome in 46,XY females.

Por Disteche, C M, Casanova, M, Saal, H, Friedman, C, Sybert, V, Graham, J, Thuline, H, Page, D C, Fellous, M
Publicado em 1986

Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?

Por Schmitt, K., Lazzeroni, L. C., Foote, S., Vollrath, D., Fisher, E. M., Goradia, T. M., Lange, K., Page, D. C., Arnheim, N.
Publicado em 1994

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Por Annerén, G, Andersson, M, Page, D C, Brown, L G, Berg, M, Läckgren, G, Gustavson, K H, de la Chapelle, A
Publicado em 1987

A deletion map of the human Y chromosome based on DNA hybridization.

Por Vergnaud, G, Page, D C, Simmler, M C, Brown, L, Rouyer, F, Noel, B, Botstein, D, de la Chapelle, A, Weissenbach, J
Publicado em 1986

Steroid sulfatase gene in XX males.

Por Mohandas, T K, Stern, H J, Meeker, C A, Passage, M B, Müller, U, Page, D C, Yen, P H, Shapiro, L J
Publicado em 1990