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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 17, 2010
[New technologies for the human genome exploration]
B Keren, C Schluth-Bolard, G Egea, et al.
The Israel Journal of Psychiatry and Related Sciences
|
January 1, 1983
Outcome of psychiatric hospitalization of Israeli soldiers in compulsory service
A B Keren, R Mester, Y Aspormas, et al.
Diabetes & Metabolism
|
November 14, 2016
Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B (HNF1B) molecular defects
D Dubois-Laforgue, C Bellanné-Chantelot, P Charles, et al.
Revue Neurologique
|
August 6, 2025
Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure
D M Chitimus, C Adam, C Cauquil, et al.
Clinical Genetics
|
August 2, 2017
Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly
A Lavillaureix, S Heide, S Chantot-Bastaraud, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
December 9, 2022
Spectrum of brain malformations in fetuses with mild tubulinopathy
R Hagege, K Krajden Haratz, G Malinger, et al.
Clinical Genetics
|
May 18, 2018
NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder
J Lévy, S Grotto, C Mignot, et al.
Journal of Medical Genetics
|
November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience
B Keren, A Hadchouel, S Saba, et al.
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.
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of 2
Search research articles
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Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 17, 2010
[New technologies for the human genome exploration]
B Keren, C Schluth-Bolard, G Egea, et al.
The Israel Journal of Psychiatry and Related Sciences
|
January 1, 1983
Outcome of psychiatric hospitalization of Israeli soldiers in compulsory service
A B Keren, R Mester, Y Aspormas, et al.
Diabetes & Metabolism
|
November 14, 2016
Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B (HNF1B) molecular defects
D Dubois-Laforgue, C Bellanné-Chantelot, P Charles, et al.
Revue Neurologique
|
August 6, 2025
Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure
D M Chitimus, C Adam, C Cauquil, et al.
Clinical Genetics
|
August 2, 2017
Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly
A Lavillaureix, S Heide, S Chantot-Bastaraud, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
December 9, 2022
Spectrum of brain malformations in fetuses with mild tubulinopathy
R Hagege, K Krajden Haratz, G Malinger, et al.
Clinical Genetics
|
May 18, 2018
NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder
J Lévy, S Grotto, C Mignot, et al.
Journal of Medical Genetics
|
November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience
B Keren, A Hadchouel, S Saba, et al.
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.
Page
of 2