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American Journal of Medical Genetics
|
July 1, 1991
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia
S M Pulst, T Pribyl, D F Barker, et al.
Nature Genetics
|
March 30, 2001
Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1
R M Costa, T Yang, D P Huynh, et al.
Archives of Neurology
|
October 27, 2001
Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia
K P Figueroa, P Chan, L Schöls, et al.
AJR. American Journal of Roentgenology
|
October 1, 1995
Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety
V F Mautner, M Tatagiba, M Lindenau, et al.
Human Genetics
|
June 1, 1991
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion
J R Korenberg, D K Kalousek, G Anneren, et al.
American Journal of Medical Genetics
|
May 1, 1993
Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores
A Nechiporuk, P Fain, E Kort, et al.
Nature Genetics
|
April 16, 1998
Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin
D R Scoles, D P Huynh, P A Morcos, et al.
Neurology
|
November 1, 1996
Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations
M E Baser, V F Mautner, N K Ragge, et al.
Journal of Neural Transmission. Supplementum
|
September 10, 2004
Screening for mutations in synaptotagmin XI in Parkinson's disease
A S Glass, D P Huynh, Th Franck, et al.
Neurosurgery
|
May 1, 1996
The neuroimaging and clinical spectrum of neurofibromatosis 2
V F Mautner, M Lindenau, M E Baser, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 106) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
July 1, 1991
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia
S M Pulst, T Pribyl, D F Barker, et al.
Nature Genetics
|
March 30, 2001
Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1
R M Costa, T Yang, D P Huynh, et al.
Archives of Neurology
|
October 27, 2001
Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia
K P Figueroa, P Chan, L Schöls, et al.
AJR. American Journal of Roentgenology
|
October 1, 1995
Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety
V F Mautner, M Tatagiba, M Lindenau, et al.
Human Genetics
|
June 1, 1991
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion
J R Korenberg, D K Kalousek, G Anneren, et al.
American Journal of Medical Genetics
|
May 1, 1993
Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores
A Nechiporuk, P Fain, E Kort, et al.
Nature Genetics
|
April 16, 1998
Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin
D R Scoles, D P Huynh, P A Morcos, et al.
Neurology
|
November 1, 1996
Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations
M E Baser, V F Mautner, N K Ragge, et al.
Journal of Neural Transmission. Supplementum
|
September 10, 2004
Screening for mutations in synaptotagmin XI in Parkinson's disease
A S Glass, D P Huynh, Th Franck, et al.
Neurosurgery
|
May 1, 1996
The neuroimaging and clinical spectrum of neurofibromatosis 2
V F Mautner, M Lindenau, M E Baser, et al.
Page
of 11