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American Journal of Medical Genetics
|
February 13, 1995
Pitt-Rogers-Danks syndrome: further delineation
L A Lizcano-Gil, D García-Cruz, O García-Cruz, et al.
Clinical Genetics
|
October 1, 1982
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies
J M Cantú, J Sánchez-Corona, A Hernándes, et al.
Annales De Genetique
|
January 1, 1986
De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome
L García-Esquivel, D García-Cruz, H Rivera, et al.
Clinical Genetics
|
September 1, 1991
Poland-Moebius syndrome in a boy and Poland syndrome in his mother
A Rojas-Martínez, D García-Cruz, A Rodríguez García, et al.
Annales De Genetique
|
January 1, 1985
Constitutional mosaic t(2;7)(q33;p22) and other rearrangements in a girl with Wilms' tumor
H Rivera, C Ruiz, D García-Cruz, et al.
Cytogenetics and Cell Genetics
|
January 1, 1984
On telomere replication and fusion in eukaryotes: apropos of a case of 45,X/46,X,ter rea(X;X)(p22.3;p22.3)
H Rivera, M T Solé, D García-Cruz, et al.
Clinical Genetics
|
September 1, 1980
Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder
J M Cantú, H Rivera, Z Nazará, et al.
American Journal of Medical Genetics
|
January 10, 1997
Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia
L A Lizcano-Gil, D García-Cruz, M del Pilar Bernal-Beltrán, et al.
Annales De Genetique
|
January 1, 1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment
D García-Cruz, L García-Esquivel, H Rivera, et al.
Clinical Genetics
|
January 1, 1993
Guadalajara camptodactyly syndrome type I. A corroborative family
L E Figuera, M L Ramírez-Dueñas, D García-Cruz, et al.
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of 6
Search research articles
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Showing results (11-20 of 54) with videos related to
Sort By:
Page
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American Journal of Medical Genetics
|
February 13, 1995
Pitt-Rogers-Danks syndrome: further delineation
L A Lizcano-Gil, D García-Cruz, O García-Cruz, et al.
Clinical Genetics
|
October 1, 1982
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies
J M Cantú, J Sánchez-Corona, A Hernándes, et al.
Annales De Genetique
|
January 1, 1986
De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome
L García-Esquivel, D García-Cruz, H Rivera, et al.
Clinical Genetics
|
September 1, 1991
Poland-Moebius syndrome in a boy and Poland syndrome in his mother
A Rojas-Martínez, D García-Cruz, A Rodríguez García, et al.
Annales De Genetique
|
January 1, 1985
Constitutional mosaic t(2;7)(q33;p22) and other rearrangements in a girl with Wilms' tumor
H Rivera, C Ruiz, D García-Cruz, et al.
Cytogenetics and Cell Genetics
|
January 1, 1984
On telomere replication and fusion in eukaryotes: apropos of a case of 45,X/46,X,ter rea(X;X)(p22.3;p22.3)
H Rivera, M T Solé, D García-Cruz, et al.
Clinical Genetics
|
September 1, 1980
Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder
J M Cantú, H Rivera, Z Nazará, et al.
American Journal of Medical Genetics
|
January 10, 1997
Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia
L A Lizcano-Gil, D García-Cruz, M del Pilar Bernal-Beltrán, et al.
Annales De Genetique
|
January 1, 1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment
D García-Cruz, L García-Esquivel, H Rivera, et al.
Clinical Genetics
|
January 1, 1993
Guadalajara camptodactyly syndrome type I. A corroborative family
L E Figuera, M L Ramírez-Dueñas, D García-Cruz, et al.
Page
of 6