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Pathologie-Biologie
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May 10, 2008
[New chromosomal syndromes]
C Schluth-Bolard, M Till, P Edery, et al.
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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 13, 2017
[Renal abnormalities in Down syndrome: A review]
C Niamien-Attai, J Bacchetta, B Ranchin, et al.
American Journal of Medical Genetics
|
March 10, 2001
No evidence of unbalanced growth-related gene inheritance in a series of overgrowth syndrome patients
L Faivre, M Vekemans, D Sanlaville, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 26, 2004
[Diagnostic approach in patients with severe and syndromic mental retardation]
M Rio, L Colleaux, D Sanlaville, et al.
Gynecologie, Obstetrique & Fertilite
|
November 15, 2011
[Trisomy 21 by isochromosome: a case report of true false negative of chorionic villi sampling]
J Caloone, D Sanlaville, A Fichez, et al.
Schizophrenia Research
|
September 13, 2016
16q12.2q21: A new susceptibility locus for schizophrenia?
A Poisson, C Schluth Bolard, B Martin, et al.
European Journal of Medical Genetics
|
September 10, 2010
Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation
C Abadie, F Bernard, I Netchine, 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.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Clinical overlap of OFD type IX with Pallister-Killian syndrome (tetrasomy 12p)
D Geneviève, Y Sznajer, M Raoul, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 6
Pathologie-Biologie
|
May 10, 2008
[New chromosomal syndromes]
C Schluth-Bolard, M Till, P Edery, et al.
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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 13, 2017
[Renal abnormalities in Down syndrome: A review]
C Niamien-Attai, J Bacchetta, B Ranchin, et al.
American Journal of Medical Genetics
|
March 10, 2001
No evidence of unbalanced growth-related gene inheritance in a series of overgrowth syndrome patients
L Faivre, M Vekemans, D Sanlaville, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 26, 2004
[Diagnostic approach in patients with severe and syndromic mental retardation]
M Rio, L Colleaux, D Sanlaville, et al.
Gynecologie, Obstetrique & Fertilite
|
November 15, 2011
[Trisomy 21 by isochromosome: a case report of true false negative of chorionic villi sampling]
J Caloone, D Sanlaville, A Fichez, et al.
Schizophrenia Research
|
September 13, 2016
16q12.2q21: A new susceptibility locus for schizophrenia?
A Poisson, C Schluth Bolard, B Martin, et al.
European Journal of Medical Genetics
|
September 10, 2010
Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation
C Abadie, F Bernard, I Netchine, 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.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Clinical overlap of OFD type IX with Pallister-Killian syndrome (tetrasomy 12p)
D Geneviève, Y Sznajer, M Raoul, et al.
Page
of 6