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C Turleau

Showing results (101-110 of 155) with videos related to

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Genomics|November 1, 1990
Assignment of a human cyclin A gene to 4q26-q27V Blanquet, J A Wang, X Chenivesse, et al.
Annales De Genetique|January 1, 1981
[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]J de Grouchy, E Thibaud, C Turleau, et al.
Human Genetics|October 1, 1986
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1C Turleau, F Taillard, M Doussau de Bazignan, et al.
American Journal of Medical Genetics|April 6, 1999
De novo inverted duplication 9p21pter involving telomeric repeated sequencesD Sanlaville, C Baumann, J M Lapierre, et al.
Annales De Genetique|January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complexC Junien, C Turleau, J de Grouchy, et al.
Human Genetics|January 1, 1984
Del11p13/nephroblastoma without aniridiaC Turleau, J de Grouchy, C Nihoul-Fékété, et al.
Bulletin Des Societes D'Ophtalmologie De France|October 1, 1981
[Intercalary deletion of the short arm of chromosome 11: aniridia, glaucoma, staturoponderal and mental retardation, sexual ambiguity, gonadoblastoma and catalase deficiency]J L Dufier, L H Phug, P Schmelck, et al.
American Journal of Medical Genetics|November 15, 2000
Chromosome 7q22-q31 duplication: report of a new case and reviewA Mégarbané, P Gosset, N Souraty, et al.
Annales De Genetique|January 1, 1988
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.
Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.
Pageof 16

Showing results (101-110 of 155) with videos related to

Sort By:
Pageof 16
Genomics|November 1, 1990
Assignment of a human cyclin A gene to 4q26-q27V Blanquet, J A Wang, X Chenivesse, et al.
Annales De Genetique|January 1, 1981
[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]J de Grouchy, E Thibaud, C Turleau, et al.
Human Genetics|October 1, 1986
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1C Turleau, F Taillard, M Doussau de Bazignan, et al.
American Journal of Medical Genetics|April 6, 1999
De novo inverted duplication 9p21pter involving telomeric repeated sequencesD Sanlaville, C Baumann, J M Lapierre, et al.
Annales De Genetique|January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complexC Junien, C Turleau, J de Grouchy, et al.
Human Genetics|January 1, 1984
Del11p13/nephroblastoma without aniridiaC Turleau, J de Grouchy, C Nihoul-Fékété, et al.
Bulletin Des Societes D'Ophtalmologie De France|October 1, 1981
[Intercalary deletion of the short arm of chromosome 11: aniridia, glaucoma, staturoponderal and mental retardation, sexual ambiguity, gonadoblastoma and catalase deficiency]J L Dufier, L H Phug, P Schmelck, et al.
American Journal of Medical Genetics|November 15, 2000
Chromosome 7q22-q31 duplication: report of a new case and reviewA Mégarbané, P Gosset, N Souraty, et al.
Annales De Genetique|January 1, 1988
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.
Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.
Pageof 16