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Annales De Genetique|June 1, 1975
[Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father]C Turleau, J De Grouchy, M Roubin, et al.Clinical Genetics|July 1, 1980
Trisomy 18q-. Trisomy mapping of chromosome 18 revisitedC Turleau, F Chavin-Colin, R Narbouton, et al.Human Genetics|May 1, 1987
De novo t(2;13)(p24.3;q14.2) and retinoblastoma. Mapping of two 13q14 probes by in situ hybridizationV Blanquet, C Turleau, N Créau-Goldberg, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1980
Ocular abnormalities of true microcephalyC Alzial, J L Dufier, J Aicardi, et al.La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 8, 1981
[Hereditary microcephaly with autosomal dominant chorioretinal dysplasia (author's transl)]C Alzial, J L Dufier, C Brasnu, et al.Annales De Genetique|January 1, 1983
Two cases of del(13q)-retinoblastoma and two cases of partial trisomy due to a familial insertionC Turleau, J de Grouchy, F Chavin-Colin, et al.Clinical Genetics|July 1, 1988
6q1 monosomy: a distinctive syndromeC Turleau, G Demay, M O Cabanis, et al.Annales De Genetique|September 1, 1978
[Del (13) (q33). Exclusion of esterase D (ESD) from 13q33 and q34]C Turleau, J Séger, J de Grouchy, et al.Annales De Genetique|December 1, 1978
[Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+]J de Grouchy, C Turleau, F Danis, et al.Human Genetics|June 10, 1977
Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriersC Turleau, F Chavin-Colin, J de Grouchy, et al.Pageof 13