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Showing results (51-60 of 61) with videos related to

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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 factorsB 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 geneV 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 outcomeB 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 familiesF 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 IS 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.
Pageof 7

Showing results (51-60 of 61) with videos related to

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Pageof 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 factorsB 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 geneV 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 outcomeB 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 familiesF 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 IS 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.
Pageof 7