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C Turleau

Showing results (71-80 of 155) with videos related to

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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.
Human Genetics|September 10, 1976
Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34M A Ferguson-Smith, D A Aitken, C Turleau, et al.
Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.
Human Genetics|January 1, 1982
Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23C Turleau, F Chavin-Colin, J de Grouchy, et al.
Annales De Genetique|September 1, 1974
[Trisomy 9p : 2 further cases]C Turleau, J de Grouchy, F Chavin-Colin, et al.
Annales De Genetique|January 1, 1982
Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3)C Junien, S Despoisse, C Turleau, et al.
Clinical Genetics|August 18, 1999
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionO Baud, V Cormier-Daire, S Lyonnet, et al.
Annales De Genetique|December 1, 1975
[Partial 11q monosomy and trigonocephaly. A new syndrome]C Turleau, F Chavin-Colin, M Roubin, et al.
Clinical Genetics|October 1, 1984
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literatureC Turleau, J de Grouchy, M F Tournade, et al.
Pageof 16

Showing results (71-80 of 155) with videos related to

Sort By:
Pageof 16
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.
Human Genetics|September 10, 1976
Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34M A Ferguson-Smith, D A Aitken, C Turleau, et al.
Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.
Human Genetics|January 1, 1982
Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23C Turleau, F Chavin-Colin, J de Grouchy, et al.
Annales De Genetique|September 1, 1974
[Trisomy 9p : 2 further cases]C Turleau, J de Grouchy, F Chavin-Colin, et al.
Annales De Genetique|January 1, 1982
Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3)C Junien, S Despoisse, C Turleau, et al.
Clinical Genetics|August 18, 1999
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionO Baud, V Cormier-Daire, S Lyonnet, et al.
Annales De Genetique|December 1, 1975
[Partial 11q monosomy and trigonocephaly. A new syndrome]C Turleau, F Chavin-Colin, M Roubin, et al.
Clinical Genetics|October 1, 1984
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literatureC Turleau, J de Grouchy, M F Tournade, et al.
Pageof 16