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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.
Pathologie-Biologie
|
May 10, 2008
[New chromosomal syndromes]
C Schluth-Bolard, M Till, P Edery, et al.
Schizophrenia Research
|
September 13, 2016
16q12.2q21: A new susceptibility locus for schizophrenia?
A Poisson, C Schluth Bolard, B Martin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 22, 2018
Detection of rare autosomal trisomies through non-invasive prenatal testing: benefits for pregnancy management
N Chatron, M Till, C Abel, et al.
Molecular Human Reproduction
|
May 19, 2021
Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders
T Yammine, N Reynaud, H Lejeune, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
September 8, 2018
Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting
L Allach El Khattabi, S Brun, P Gueguen, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
April 14, 2017
Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital
L Pons, M Till, E Alix, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
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.
Pathologie-Biologie
|
May 10, 2008
[New chromosomal syndromes]
C Schluth-Bolard, M Till, P Edery, et al.
Schizophrenia Research
|
September 13, 2016
16q12.2q21: A new susceptibility locus for schizophrenia?
A Poisson, C Schluth Bolard, B Martin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 22, 2018
Detection of rare autosomal trisomies through non-invasive prenatal testing: benefits for pregnancy management
N Chatron, M Till, C Abel, et al.
Molecular Human Reproduction
|
May 19, 2021
Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders
T Yammine, N Reynaud, H Lejeune, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
September 8, 2018
Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting
L Allach El Khattabi, S Brun, P Gueguen, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
April 14, 2017
Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital
L Pons, M Till, E Alix, et al.
Page
of 1