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American Journal of Human Genetics
|
August 1, 1990
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
J R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics
|
June 19, 1998
A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique
E Sidransky, C Burgess, T Ikeuchi, et al.
Genomics
|
April 1, 1996
A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21
M Ohira, H Ichikawa, E Suzuki, et al.
Transplantation
|
November 4, 2000
The prevalence of TT virus infection in renal transplant recipients in Brazil
O Yokosuka, T Ikeuchi, T Kanda, et al.
Journal of Neurology
|
February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasia
S N Illarioshkin, K M Allen, J G Gleeson, et al.
European Journal of Neurology
|
September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation
T Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology
|
September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation
T Konno, K Yoshida, T Mizuno, et al.
Journal of the Neurological Sciences
|
September 19, 1998
Phenotype variation correlates with CAG repeat length in SCA2--a study of 28 Japanese patients
H Sasaki, A Wakisaka, K Sanpei, et al.
European Journal of Neurology
|
March 7, 2018
Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities
T Konno, T Miura, A M Harriott, et al.
The Journal of Prevention of Alzheimer'S Disease
|
January 15, 2025
Cutting through the noise: A narrative review of Alzheimer's disease plasma biomarkers for routine clinical use
M Schöll, A Vrillon, T Ikeuchi, et al.
Page
of 31
Search research articles
Search
Showing results (271-280 of 303) with videos related to
Sort By:
Page
of 31
American Journal of Human Genetics
|
August 1, 1990
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
J R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics
|
June 19, 1998
A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique
E Sidransky, C Burgess, T Ikeuchi, et al.
Genomics
|
April 1, 1996
A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21
M Ohira, H Ichikawa, E Suzuki, et al.
Transplantation
|
November 4, 2000
The prevalence of TT virus infection in renal transplant recipients in Brazil
O Yokosuka, T Ikeuchi, T Kanda, et al.
Journal of Neurology
|
February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasia
S N Illarioshkin, K M Allen, J G Gleeson, et al.
European Journal of Neurology
|
September 19, 2017
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation
T Konno, K Yoshida, I Mizuta, et al.
European Journal of Neurology
|
September 30, 2016
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation
T Konno, K Yoshida, T Mizuno, et al.
Journal of the Neurological Sciences
|
September 19, 1998
Phenotype variation correlates with CAG repeat length in SCA2--a study of 28 Japanese patients
H Sasaki, A Wakisaka, K Sanpei, et al.
European Journal of Neurology
|
March 7, 2018
Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities
T Konno, T Miura, A M Harriott, et al.
The Journal of Prevention of Alzheimer'S Disease
|
January 15, 2025
Cutting through the noise: A narrative review of Alzheimer's disease plasma biomarkers for routine clinical use
M Schöll, A Vrillon, T Ikeuchi, et al.
Page
of 31