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Annales De Genetique|January 1, 1979
[Sex linked mental deficiency, unusual facies, macroorchidism and fragile site on chromosome X (author's transl)]C Turleau, P Czernichow, R Gorin, et al.
Annales De Genetique|June 1, 1977
[Ring of the chromosome 4. II. Without facial dysmorphism]F Chavin-Colin, C Turleau, J M Limal, et al.
American Journal of Medical Genetics|January 1, 1990
Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome XH Journel, J Melki, C Turleau, et al.
Annales De Genetique|January 1, 1979
[46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)]C Turleau, M O Rethoré, C Junien, 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.
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|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.
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