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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
August 10, 2010
[Tetragametic chimerism: Case report]
A Loriaux, S Boulet, V Delorme, et al.
European Journal of Epidemiology
|
April 29, 1998
Cytomegalovirus seroprevalence in French pregnant women: parity and place of birth as major predictive factors
B Gratacap-Cavallier, J L Bosson, P Morand, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 7, 2015
[Schooling and care of mild intellectual disability children]
M David, A Billette de Villemeur, F Devillard, et al.
Annales De Genetique
|
December 8, 2004
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)
J Lespinasse, H Testard, F Nugues, et al.
American Journal of Human Genetics
|
June 12, 1999
Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene
V Satre, N Monnier, F Berthoin, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
May 26, 1998
[Cytomegalovirus infection in pregnant women. Seroepidemiological prospective study in 1,018 women in Isere]
B Gratacap-Cavallier, P Morand, N Dutertre, et al.
European Journal of Medical Genetics
|
November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome
B Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Clinical Genetics
|
June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families
F Petit, A-S Jourdain, J Andrieux, et al.
Clinical Genetics
|
October 13, 2009
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I
S Saal, L Faivre, Bernard Aral, et al.
Clinical Genetics
|
October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?
S El Chehadeh, R Touraine, F Prieur, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
August 10, 2010
[Tetragametic chimerism: Case report]
A Loriaux, S Boulet, V Delorme, et al.
European Journal of Epidemiology
|
April 29, 1998
Cytomegalovirus seroprevalence in French pregnant women: parity and place of birth as major predictive factors
B Gratacap-Cavallier, J L Bosson, P Morand, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 7, 2015
[Schooling and care of mild intellectual disability children]
M David, A Billette de Villemeur, F Devillard, et al.
Annales De Genetique
|
December 8, 2004
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)
J Lespinasse, H Testard, F Nugues, et al.
American Journal of Human Genetics
|
June 12, 1999
Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene
V Satre, N Monnier, F Berthoin, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
May 26, 1998
[Cytomegalovirus infection in pregnant women. Seroepidemiological prospective study in 1,018 women in Isere]
B Gratacap-Cavallier, P Morand, N Dutertre, et al.
European Journal of Medical Genetics
|
November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome
B Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Clinical Genetics
|
June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families
F Petit, A-S Jourdain, J Andrieux, et al.
Clinical Genetics
|
October 13, 2009
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I
S Saal, L Faivre, Bernard Aral, et al.
Clinical Genetics
|
October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?
S El Chehadeh, R Touraine, F Prieur, et al.
Page
of 7