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American Journal of Medical Genetics
|
June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndrome
A E Lin, Q Liu, G B Mannheim, et al.
American Journal of Human Genetics
|
August 1, 1989
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13
U Francke, B T Darras, N F Zander, et al.
Journal of Neuro-Oncology
|
January 1, 1993
Aggressive oligodendroglioma predicted by chromosome 10 restriction fragment length polymorphism analysis. Case study
J K Wu, R D Folkerth, Z Ye, et al.
Brain & Development
|
July 1, 1992
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndrome
M J Rivkin, Z Ye, G B Mannheim, et al.
Pediatric Neurology
|
July 9, 2010
Electrophysiologic evidence for anterior horn cell disease in amyoplasia
John N Gaitanis, Hugh J McMillan, Allan Wu, et al.
Neurology
|
July 13, 2012
Machine learning algorithms to classify spinal muscular atrophy subtypes
Tuhin Srivastava, Basil T Darras, Jim S Wu, et al.
Genomics
|
May 1, 1991
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenes
M I Lomax, C L Hsieh, B T Darras, et al.
Journal Belge De Radiologie
|
January 1, 1977
Endoscopic retrograde pancreatography in the diagnosis of pancreatico-pleural fistula
T Darras, A Gulbis, E Khazzaka, et al.
Chest
|
June 1, 1972
Intermittent therapy with rifampin once a week in advanced pulmonary tuberculosis
L Verbist, S Mbete, H Van Landuyt, et al.
The New England Journal of Medicine
|
July 2, 2025
Further Comments on Risdiplam for Prenatal Therapy of Spinal Muscular Atrophy
Crystal J J Yeo, Darryl C De Vivo, Basil T Darras
Page
of 31
Search research articles
Search
Showing results (81-90 of 303) with videos related to
Sort By:
Page
of 31
American Journal of Medical Genetics
|
June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndrome
A E Lin, Q Liu, G B Mannheim, et al.
American Journal of Human Genetics
|
August 1, 1989
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13
U Francke, B T Darras, N F Zander, et al.
Journal of Neuro-Oncology
|
January 1, 1993
Aggressive oligodendroglioma predicted by chromosome 10 restriction fragment length polymorphism analysis. Case study
J K Wu, R D Folkerth, Z Ye, et al.
Brain & Development
|
July 1, 1992
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndrome
M J Rivkin, Z Ye, G B Mannheim, et al.
Pediatric Neurology
|
July 9, 2010
Electrophysiologic evidence for anterior horn cell disease in amyoplasia
John N Gaitanis, Hugh J McMillan, Allan Wu, et al.
Neurology
|
July 13, 2012
Machine learning algorithms to classify spinal muscular atrophy subtypes
Tuhin Srivastava, Basil T Darras, Jim S Wu, et al.
Genomics
|
May 1, 1991
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenes
M I Lomax, C L Hsieh, B T Darras, et al.
Journal Belge De Radiologie
|
January 1, 1977
Endoscopic retrograde pancreatography in the diagnosis of pancreatico-pleural fistula
T Darras, A Gulbis, E Khazzaka, et al.
Chest
|
June 1, 1972
Intermittent therapy with rifampin once a week in advanced pulmonary tuberculosis
L Verbist, S Mbete, H Van Landuyt, et al.
The New England Journal of Medicine
|
July 2, 2025
Further Comments on Risdiplam for Prenatal Therapy of Spinal Muscular Atrophy
Crystal J J Yeo, Darryl C De Vivo, Basil T Darras
Page
of 31