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Human Genetics|September 1, 1990
Frequency of the major CF mutation in French CF patientsJ C Chomel, A Haliassos, L Tesson, et al.Leukemia & Lymphoma|November 8, 2001
Persistence of transcriptionally silent BCR-ABL rearrangements in chronic myeloid leukemia patients in sustained complete cytogenetic remissionA Kitzis, F Brizard, C Dascalescu, et al.Prenatal Diagnosis|April 1, 1989
Usefulness of linkage disequilibrium of KM-19 and XV-2c DNA probes for genetic counselling in a high-risk CF familyJ C Chomel, A Haliassos, L Tesson, et al.Nucleic Acids Research|October 25, 1989
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markersA Haliassos, J C Chomel, S Grandjouan, et al.Platelets|October 27, 2009
Stroke and aspirin non-responder patients: relation with hypertension and platelet response to adenosine diphosphateG Godeneche, N Sorel, S Ragot, et al.Human Molecular Genetics|January 1, 1993
Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patientsS Akli, J C Chomel, J M Lacorte, et al.Annales De Biologie Clinique|January 1, 1989
[Establishment of a range of phtalate density for studying profiles of erythrocyte density]J C Chomel, K Cherara, D Vanhaeke, et al.Leukemia|April 7, 1998
Identification of several genes differentially expressed during progression of chronic myelogenous leukemiaL Dahéron, S Salmeron, S Patri, et al.Human Genetics|March 1, 1992
CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcriptsN Fonknechten, J Chelly, J Lepercq, et al.Human Genetics|August 1, 1995
A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23P Amati, J C Chomel, A Nivelon-Chevalier, et al.Pageof 2