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Investigative Ophthalmology & Visual Science
|
September 28, 2000
A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family
E Pras, M Frydman, E Levy-Nissenbaum, et al.
Nature
|
March 8, 1990
A single origin of phenylketonuria in Yemenite Jews
S Avigad, B E Cohen, S Bauer, et al.
The Journal of Pediatrics
|
September 1, 1993
Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant
O P Hamiel, A Raas-Rothschild, M Upadhyaya, et al.
Schizophrenia Research
|
February 16, 1999
Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome
D Gothelf, A Frisch, H Munitz, et al.
American Journal of Medical Genetics
|
December 31, 1997
Velocardiofacial manifestations and microdeletions in schizophrenic inpatients
D Gothelf, A Frisch, H Munitz, et al.
Journal of Medicinal Chemistry
|
August 12, 2021
Discovery of an Orally Bioavailable Small-Molecule Inhibitor for the β-Catenin/B-Cell Lymphoma 9 Protein-Protein Interaction
Zhen Wang, Min Zhang, Victor Quereda, et al.
American Journal of Medical Genetics
|
October 1, 1992
Rambam-Hasharon syndrome of psychomotor retardation, short stature, defective neutrophil motility, and Bombay phenotype
M Frydman, A Etzioni, T Eidlitz-Markus, et al.
The Journal of Antimicrobial Chemotherapy
|
July 1, 1988
Pharmacokinetics of spiramycin in man
A M Frydman, Y Le Roux, J F Desnottes, et al.
Journal of the Chemical Society. Perkin Transactions 1
|
January 1, 1976
Fungal products. Part XVII. Microbiological hydroxylation of gibberellin A9 and its methyl ester
J R Bearder, V M Frydman, P Gaskin, et al.
Mbio
|
May 24, 2018
<i>Wolbachia w</i>Stri Blocks Zika Virus Growth at Two Independent Stages of Viral Replication
M J Schultz, A L Tan, C N Gray, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 172) with videos related to
Sort By:
Page
of 18
Investigative Ophthalmology & Visual Science
|
September 28, 2000
A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family
E Pras, M Frydman, E Levy-Nissenbaum, et al.
Nature
|
March 8, 1990
A single origin of phenylketonuria in Yemenite Jews
S Avigad, B E Cohen, S Bauer, et al.
The Journal of Pediatrics
|
September 1, 1993
Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant
O P Hamiel, A Raas-Rothschild, M Upadhyaya, et al.
Schizophrenia Research
|
February 16, 1999
Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome
D Gothelf, A Frisch, H Munitz, et al.
American Journal of Medical Genetics
|
December 31, 1997
Velocardiofacial manifestations and microdeletions in schizophrenic inpatients
D Gothelf, A Frisch, H Munitz, et al.
Journal of Medicinal Chemistry
|
August 12, 2021
Discovery of an Orally Bioavailable Small-Molecule Inhibitor for the β-Catenin/B-Cell Lymphoma 9 Protein-Protein Interaction
Zhen Wang, Min Zhang, Victor Quereda, et al.
American Journal of Medical Genetics
|
October 1, 1992
Rambam-Hasharon syndrome of psychomotor retardation, short stature, defective neutrophil motility, and Bombay phenotype
M Frydman, A Etzioni, T Eidlitz-Markus, et al.
The Journal of Antimicrobial Chemotherapy
|
July 1, 1988
Pharmacokinetics of spiramycin in man
A M Frydman, Y Le Roux, J F Desnottes, et al.
Journal of the Chemical Society. Perkin Transactions 1
|
January 1, 1976
Fungal products. Part XVII. Microbiological hydroxylation of gibberellin A9 and its methyl ester
J R Bearder, V M Frydman, P Gaskin, et al.
Mbio
|
May 24, 2018
<i>Wolbachia w</i>Stri Blocks Zika Virus Growth at Two Independent Stages of Viral Replication
M J Schultz, A L Tan, C N Gray, et al.
Page
of 18