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AJNR. American Journal of Neuroradiology
|
December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations
M Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
FEBS Letters
|
August 28, 1998
Expression of the SOX10 gene during human development
N Bondurand, A Kobetz, V Pingault, et al.
Clinical Genetics
|
April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
C T Gordon, A Tessier, Z Demir, et al.
Human Molecular Genetics
|
August 11, 1999
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
N Bondurand, K Kuhlbrodt, V Pingault, et al.
Clinical Genetics
|
September 27, 2014
SOX10 mutations mimic isolated hearing loss
V Pingault, E Faubert, V Baral, et al.
The Medical Journal of Australia
|
April 28, 2025
Nirsevimab immunisation of infants and respiratory syncytial virus (RSV)-associated hospitalisations, Western Australia, 2024: a population-based analysis
Lauren E Bloomfield, Nevada V Pingault, Rachel E Foong, et al.
American Journal of Human Genetics
|
April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain
R L Touraine, T Attié-Bitach, E Manceau, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2022
SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients
M Mouillé, M Rio, S Breton, et al.
Nature Genetics
|
February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
V Pingault, N Bondurand, K Kuhlbrodt, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
AJNR. American Journal of Neuroradiology
|
December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations
M Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
FEBS Letters
|
August 28, 1998
Expression of the SOX10 gene during human development
N Bondurand, A Kobetz, V Pingault, et al.
Clinical Genetics
|
April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
C T Gordon, A Tessier, Z Demir, et al.
Human Molecular Genetics
|
August 11, 1999
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
N Bondurand, K Kuhlbrodt, V Pingault, et al.
Clinical Genetics
|
September 27, 2014
SOX10 mutations mimic isolated hearing loss
V Pingault, E Faubert, V Baral, et al.
The Medical Journal of Australia
|
April 28, 2025
Nirsevimab immunisation of infants and respiratory syncytial virus (RSV)-associated hospitalisations, Western Australia, 2024: a population-based analysis
Lauren E Bloomfield, Nevada V Pingault, Rachel E Foong, et al.
American Journal of Human Genetics
|
April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain
R L Touraine, T Attié-Bitach, E Manceau, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2022
SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients
M Mouillé, M Rio, S Breton, et al.
Nature Genetics
|
February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
V Pingault, N Bondurand, K Kuhlbrodt, et al.
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of 2