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Translational Psychiatry
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October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
C Nava, F Lamari, D Héron, et al.
Clinical Genetics
|
July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients
E Chérot, B Keren, C Dubourg, et al.
International Journal of Obesity (2005)
|
December 2, 2015
16p11.2 Locus modulates response to satiety before the onset of obesity
A M Maillard, L Hippolyte, B Rodriguez-Herreros, et al.
European Journal of Neurology
|
June 20, 2020
Deciphering the natural history of SCA7 in children
M G Bah, D Rodriguez, C Cazeneuve, et al.
Rhinology
|
July 14, 2025
Olfactory implants: international opinion paper on emerging technologies and clinical applications
K L Whitcroft, A K Hernandez, P Andrews, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
Genetics in Medicine Open
|
December 13, 2024
<i>ARID1B</i>-related disorder in 87 adults: Natural history and self-sustainability
P J van der Sluijs, M Gösgens, A J M Dingemans, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Translational Psychiatry
|
October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
C Nava, F Lamari, D Héron, et al.
Clinical Genetics
|
July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients
E Chérot, B Keren, C Dubourg, et al.
International Journal of Obesity (2005)
|
December 2, 2015
16p11.2 Locus modulates response to satiety before the onset of obesity
A M Maillard, L Hippolyte, B Rodriguez-Herreros, et al.
European Journal of Neurology
|
June 20, 2020
Deciphering the natural history of SCA7 in children
M G Bah, D Rodriguez, C Cazeneuve, et al.
Rhinology
|
July 14, 2025
Olfactory implants: international opinion paper on emerging technologies and clinical applications
K L Whitcroft, A K Hernandez, P Andrews, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
Genetics in Medicine Open
|
December 13, 2024
<i>ARID1B</i>-related disorder in 87 adults: Natural history and self-sustainability
P J van der Sluijs, M Gösgens, A J M Dingemans, et al.
Page
of 4