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Heliyon
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November 25, 2024
A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling
C Quadalti, M Sannia, N E Humphreys, et al.
Neuroscience
|
March 23, 2016
Visual impairment in FOXG1-mutated individuals and mice
E M Boggio, L Pancrazi, M Gennaro, et al.
Environmental Research
|
June 30, 2018
Effects of carbon and silicon nanotubes and carbon nanofibers on marine microalgae Heterosigma akashiwo
K S Pikula, A M Zakharenko, V V Chaika, et al.
Clinical Genetics
|
November 19, 2016
Alport syndrome: impact of digenic inheritance in patients management
C Fallerini, M Baldassarri, E Trevisson, et al.
Human Mutation
|
February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome
T M Neri, P Zanelli, G De Palma, et al.
Brain & Development
|
April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria
R Artuso, M A Mencarelli, R Polli, et al.
American Journal of Medical Genetics
|
November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome
A Renieri, L Galli, A Grillo, et al.
American Journal of Human Genetics
|
June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
A Renieri, M Bruttini, L Galli, et al.
Journal of Medical Genetics
|
July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome
M A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
M Vacca, F Filippini, A Budillon, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 106) with videos related to
Sort By:
Page
of 11
Heliyon
|
November 25, 2024
A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling
C Quadalti, M Sannia, N E Humphreys, et al.
Neuroscience
|
March 23, 2016
Visual impairment in FOXG1-mutated individuals and mice
E M Boggio, L Pancrazi, M Gennaro, et al.
Environmental Research
|
June 30, 2018
Effects of carbon and silicon nanotubes and carbon nanofibers on marine microalgae Heterosigma akashiwo
K S Pikula, A M Zakharenko, V V Chaika, et al.
Clinical Genetics
|
November 19, 2016
Alport syndrome: impact of digenic inheritance in patients management
C Fallerini, M Baldassarri, E Trevisson, et al.
Human Mutation
|
February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome
T M Neri, P Zanelli, G De Palma, et al.
Brain & Development
|
April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria
R Artuso, M A Mencarelli, R Polli, et al.
American Journal of Medical Genetics
|
November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome
A Renieri, L Galli, A Grillo, et al.
American Journal of Human Genetics
|
June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
A Renieri, M Bruttini, L Galli, et al.
Journal of Medical Genetics
|
July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome
M A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
M Vacca, F Filippini, A Budillon, et al.
Page
of 11