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C Turleau

Showing results (61-70 of 155) with videos related to

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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.
Archives Francaises De Pediatrie|November 1, 1979
[Syndrome 48,XXXX]J de Grouchy, J Vialatte, 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.
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 Dermatologie Et De Venereologie|January 1, 1988
[Cytogenetic study of 3 cases of multiple cutaneous leiomyomatosis]C Turleau, P Y Venencie, M Roubin, et al.
Human Genetics|January 1, 1984
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8J de Grouchy, M D Dautzenberg, C Turleau, et al.
Annales De Genetique|January 1, 1985
Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric regionJ de Grouchy, C Turleau, M Doussau de Bazignan, et al.
Pageof 16

Showing results (61-70 of 155) with videos related to

Sort By:
Pageof 16
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.
Archives Francaises De Pediatrie|November 1, 1979
[Syndrome 48,XXXX]J de Grouchy, J Vialatte, 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.
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 Dermatologie Et De Venereologie|January 1, 1988
[Cytogenetic study of 3 cases of multiple cutaneous leiomyomatosis]C Turleau, P Y Venencie, M Roubin, et al.
Human Genetics|January 1, 1984
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8J de Grouchy, M D Dautzenberg, C Turleau, et al.
Annales De Genetique|January 1, 1985
Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric regionJ de Grouchy, C Turleau, M Doussau de Bazignan, et al.
Pageof 16