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Annales De Genetique|September 1, 1976
[Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility]C Turleau, M F Croquette, J C Fourlinnie, et al.
Annales De Genetique|January 1, 1996
Molecular genetics of hereditary elliptocytosis and hereditary spherocytosisJ Delaunay, N Alloisio, L Morle, et al.
Annales De Genetique|January 1, 1996
Localization of TEC to 9q22.3-q31 by fluorescence in situ hybridizationP Kleinfinger, Y Labelle, T Melot, et al.
Annales De Genetique|September 1, 1977
[H1 histone - giemsa competition and chromosome labeling]M Deminatti, J B Savary, F Strozyk
Annales De Genetique|January 1, 1996
[Genetic control of limb development]Y Hérault, D Duboule
Annales De Genetique|January 1, 1996
Trisomy X: ACLF (Association des Cytogénéticiens de Langue Française) retrospective studyA Guichet, S Briault, C Moraine, et al.
Annales De Genetique|January 1, 1996
Chromosome 22 marker in a child with Duane syndrome and urogenital abnormalitiesM G Tibiletti, E Sala, D Colombo, et al.
Annales De Genetique|January 1, 1996
Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24G J Halpern, M Shohat, P Merlob
Annales De Genetique|January 1, 1996
Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridizationM T Darnaude, A Diaz de Bustamante, P Cabello, et al.
Annales De Genetique|January 1, 1996
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian speciesC Pêcheux, A L Gall, J C Kaplan, et al.
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