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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 1, 1984
Bromocriptine in the management of end of dose deterioration in Parkinson's disease
J D Grimes, D B King, O S Kofman, et al.
Plos One
|
April 25, 2013
New system for digital to analog transformation and reconstruction of 12-lead ECGs
Roshni Kothadia, Walter B Kulecz, Igor S Kofman, et al.
Human Genetics
|
January 1, 1981
Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype
S Kofman, G Pérez-Palacios, M Medina, et al.
American Journal of Medical Genetics
|
June 13, 1997
Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region
R Coral-Vazquez, D Arenas, B Cisneros, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
January 1, 1993
[Cytogenetic study of 22 adults and 3 children with acute lymphoblastic leukemia]
R M Arana-Trejo, A Cervantes-Peredo, E Rozen, et al.
Frontiers in Systems Neuroscience
|
March 28, 2017
Functional Brain Activation in Response to a Clinical Vestibular Test Correlates with Balance
Fatemeh Noohi, Catherine Kinnaird, Yiri DeDios, et al.
American Journal of Medical Genetics
|
March 25, 1998
Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome
M López, P Canto, M Aguinaga, et al.
American Journal of Medical Genetics
|
August 22, 2000
Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA
A L Jiménez, S Kofman-Alfaro, J Berumen, et al.
Clinical Endocrinology
|
August 26, 1998
Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene
G Maya-Núñez, S Cuevas-Covarrubias, J C Zenteno, et al.
Acta Endocrinologica
|
September 1, 1981
Inherited male pseudohermaphroditism due to gonadotrophin unresponsiveness
G Pérez-Palacios, H E Scaglia, S Kofman-Alfaro, et al.
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of 10
Search research articles
Search
Showing results (41-50 of 96) with videos related to
Sort By:
Page
of 10
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 1, 1984
Bromocriptine in the management of end of dose deterioration in Parkinson's disease
J D Grimes, D B King, O S Kofman, et al.
Plos One
|
April 25, 2013
New system for digital to analog transformation and reconstruction of 12-lead ECGs
Roshni Kothadia, Walter B Kulecz, Igor S Kofman, et al.
Human Genetics
|
January 1, 1981
Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype
S Kofman, G Pérez-Palacios, M Medina, et al.
American Journal of Medical Genetics
|
June 13, 1997
Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region
R Coral-Vazquez, D Arenas, B Cisneros, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
January 1, 1993
[Cytogenetic study of 22 adults and 3 children with acute lymphoblastic leukemia]
R M Arana-Trejo, A Cervantes-Peredo, E Rozen, et al.
Frontiers in Systems Neuroscience
|
March 28, 2017
Functional Brain Activation in Response to a Clinical Vestibular Test Correlates with Balance
Fatemeh Noohi, Catherine Kinnaird, Yiri DeDios, et al.
American Journal of Medical Genetics
|
March 25, 1998
Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome
M López, P Canto, M Aguinaga, et al.
American Journal of Medical Genetics
|
August 22, 2000
Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA
A L Jiménez, S Kofman-Alfaro, J Berumen, et al.
Clinical Endocrinology
|
August 26, 1998
Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene
G Maya-Núñez, S Cuevas-Covarrubias, J C Zenteno, et al.
Acta Endocrinologica
|
September 1, 1981
Inherited male pseudohermaphroditism due to gonadotrophin unresponsiveness
G Pérez-Palacios, H E Scaglia, S Kofman-Alfaro, et al.
Page
of 10