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Nucleic Acids Research
|
February 25, 1992
Dinucleotide repeat polymorphism at the D9S121 locus (9q31-34)
D J Kwiatkowski, J F Gusella
Nucleic Acids Research
|
February 25, 1992
Dinucleotide repeat polymorphism at the D9S123 locus (9q31-34)
D J Kwaitkowski, J F Gusella
Current Opinion in Neurobiology
|
August 4, 1998
Huntingtin: a single bait hooks many species
J F Gusella, M E MacDonald
Molecular Medicine (Cambridge, Mass.)
|
April 1, 1997
The genetic defect causing Huntington's disease: repeated in other contexts?
J F Gusella, F Persichetti, M E MacDonald
Blood
|
October 1, 1984
Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells
M D Minden, J F Gusella, D Housman
Advances in Neurology
|
January 1, 1988
Molecular genetic strategies to investigate Huntington's disease
T C Gilliam, J F Gusella, H Lehrach
Neuron
|
April 16, 1998
Molecular neurobiology and genetics: investigation of neural function and dysfunction
T Green, S F Heinemann, J F Gusella
Molecular Biology & Medicine
|
February 1, 1991
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency
V Ramesh, J F Gusella, V E Shih
Nucleic Acids Research
|
December 25, 1989
MspI RFLP for human MAOA gene
L Ozelius, J F Gusella, X O Breakefield
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors
D N Louis, V Ramesh, J F Gusella
Page
of 32
Search research articles
Search
Showing results (31-40 of 313) with videos related to
Sort By:
Page
of 32
Nucleic Acids Research
|
February 25, 1992
Dinucleotide repeat polymorphism at the D9S121 locus (9q31-34)
D J Kwiatkowski, J F Gusella
Nucleic Acids Research
|
February 25, 1992
Dinucleotide repeat polymorphism at the D9S123 locus (9q31-34)
D J Kwaitkowski, J F Gusella
Current Opinion in Neurobiology
|
August 4, 1998
Huntingtin: a single bait hooks many species
J F Gusella, M E MacDonald
Molecular Medicine (Cambridge, Mass.)
|
April 1, 1997
The genetic defect causing Huntington's disease: repeated in other contexts?
J F Gusella, F Persichetti, M E MacDonald
Blood
|
October 1, 1984
Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells
M D Minden, J F Gusella, D Housman
Advances in Neurology
|
January 1, 1988
Molecular genetic strategies to investigate Huntington's disease
T C Gilliam, J F Gusella, H Lehrach
Neuron
|
April 16, 1998
Molecular neurobiology and genetics: investigation of neural function and dysfunction
T Green, S F Heinemann, J F Gusella
Molecular Biology & Medicine
|
February 1, 1991
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency
V Ramesh, J F Gusella, V E Shih
Nucleic Acids Research
|
December 25, 1989
MspI RFLP for human MAOA gene
L Ozelius, J F Gusella, X O Breakefield
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors
D N Louis, V Ramesh, J F Gusella
Page
of 32