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Genome Research|July 1, 1998
Evidence for the presence of insulin-dependent diabetes-associated alleles on the distal part of mouse chromosome 6E Melanitou, F Joly, M Lathrop, et al.
Molecular and Cellular Biology|November 24, 1999
Functional analysis of the DXPas34 locus, a 3' regulator of Xist expressionE Debrand, C Chureau, D Arnaud, et al.
Developments in Biological Standardization|January 1, 1984
Monoclonal antibodies against the human factor VIII von Willebrand molecule: characterization and potential for screening of von Willebrand patientsP Avner, D Arnaud, Y Sultan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1987
Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse crossP Avner, L Amar, D Arnaud, et al.
Comptes Rendus Des Seances De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 18, 1981
[Monoclonal antibodies against the factor VIII/Willebrand factor molecule: inhibition of the cofactor action of ristocetin and the antihemophilic factor]B Sola, P Avner, Y Sultan, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 1, 1977
Mechanism of isoproterenol-induced desensitization of tracheal smooth muscleC S Lin, L Hurwitz, J Jenne, et al.
Thrombosis and Haemostasis|December 29, 1984
An immunoradiometric assay for factor VIII related antigen (VIIIRAg) using two monoclonal antibodies-comparison with polyclonal rabbit antibodies for use in von Willebrand's disease diagnosisY Sultan, P Avner, P Maisonneuve, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
Isolation of monochromosomal hybrids for mouse chromosomes 3, 6, 10, 12, 14, and 18A Sabile, I Poras, D Cherif, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Improvement of FISH mapping resolution on combed DNA molecules by iterative constrained deconvolution: a quantitative studyK Monier, L Heliot, C Rougeulle, et al.
American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.
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