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S Gilgenkrantz

Showing results (31-40 of 129) with videos related to

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Human Genetics|January 1, 1981
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three membersS Gilgenkrantz, C Defeche, S Stehlin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1970
[Holt-Oram syndrome and hand malformations associated with congenital heart disease]C Pernot, C Dupuis, S Gilgenkrantz, et al.
Human Genetics|June 1, 1989
Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH lociG Keyeux, S Gilgenkrantz, G Lefranc, et al.
Journal De Genetique Humaine|January 1, 1988
[Y chromosome rearrangement and phenotypical consequences]P Mujica, N Abbadi, L D Formiga, et al.
Annales De Pediatrie|April 2, 1971
[A case of erythroderma ichthyosiforme congenitum associated with various abnormalities]J Castanier, P Hee, C Lelièvre-Gassin, et al.
La Presse Medicale|October 10, 1970
[A new case of XYY syndrome]F Streiff, S Gilgenkrantz, M Beaudoin, et al.
Annales De Genetique|January 1, 1985
[Union of 2 carriers of a balanced translocation. Familial study of 3 generations]S Gilgenkrantz, M J Grégoire, M Chery, et al.
Human Genetics|October 1, 1990
Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplicationG Keyeux, S Gilgenkrantz, G Lefranc, et al.
Human Genetics|January 1, 1982
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)R A Pfeiffer, R Ott, S Gilgenkrantz, et al.
Pediatrie|March 1, 1975
[Klinefelter's syndrome. Trilogy of Fallot. Teratoma of the mediastinum and early puberty]M Pierson, S Gilgenkrantz, M Saborio, et al.
Pageof 13

Showing results (31-40 of 129) with videos related to

Sort By:
Pageof 13
Human Genetics|January 1, 1981
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three membersS Gilgenkrantz, C Defeche, S Stehlin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1970
[Holt-Oram syndrome and hand malformations associated with congenital heart disease]C Pernot, C Dupuis, S Gilgenkrantz, et al.
Human Genetics|June 1, 1989
Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH lociG Keyeux, S Gilgenkrantz, G Lefranc, et al.
Journal De Genetique Humaine|January 1, 1988
[Y chromosome rearrangement and phenotypical consequences]P Mujica, N Abbadi, L D Formiga, et al.
Annales De Pediatrie|April 2, 1971
[A case of erythroderma ichthyosiforme congenitum associated with various abnormalities]J Castanier, P Hee, C Lelièvre-Gassin, et al.
La Presse Medicale|October 10, 1970
[A new case of XYY syndrome]F Streiff, S Gilgenkrantz, M Beaudoin, et al.
Annales De Genetique|January 1, 1985
[Union of 2 carriers of a balanced translocation. Familial study of 3 generations]S Gilgenkrantz, M J Grégoire, M Chery, et al.
Human Genetics|October 1, 1990
Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplicationG Keyeux, S Gilgenkrantz, G Lefranc, et al.
Human Genetics|January 1, 1982
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)R A Pfeiffer, R Ott, S Gilgenkrantz, et al.
Pediatrie|March 1, 1975
[Klinefelter's syndrome. Trilogy of Fallot. Teratoma of the mediastinum and early puberty]M Pierson, S Gilgenkrantz, M Saborio, et al.
Pageof 13