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Human Genetics
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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 members
S 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 loci
G 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 duplication
G 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.
Page
of 13
Search research articles
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Showing results (31-40 of 129) with videos related to
Sort By:
Page
of 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 members
S 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 loci
G 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 duplication
G 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.
Page
of 13