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Human Genetics|June 1, 1990
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndromeD Damiani, A E Billerbeck, A C Goldberg, et al.
Prenatal Diagnosis|July 1, 1986
Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probesS Gilgenkrantz, P Droulle, E Seboun, et al.
Atherosclerosis|July 27, 2001
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrationsD J Gaughan, L A Kluijtmans, S Barbaux, et al.
The Journal of Cell Biology|November 17, 1998
Interferon alpha inhibits a Src-mediated pathway necessary for Shigella-induced cytoskeletal rearrangements in epithelial cellsG Duménil, J C Olivo, S Pellegrini, et al.
Bulletin De L'Association Des Anatomistes|March 1, 1991
[Genetic factor of sex determination]N Abbas, J Toublanc, R Rappaport, et al.
Immunogenetics|August 26, 1998
CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybridsA M Lennon, C Ottone, M Rosemblatt, et al.
Research in Immunology|November 1, 1991
The recombinant human interferon-gamma receptor is fully functional in a human x murine hybrid containing human chromosome 21M R Bono, C Alcaïde-Loridan, B Letouzé, et al.
Annals of Human Genetics|December 4, 2003
SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery diseaseD A Tregouet, S Barbaux, O Poirier, et al.
American Journal of Human Genetics|June 1, 1996
A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndromeA Ion, L Telvi, J L Chaussain, et al.
Cytogenetics and Cell Genetics|September 8, 1998
The INSL4 gene maps close to WI-5527 at 9p24.1-->p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndromeR Veitia, A Laurent, L Quintana-Murci, et al.
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