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P Khau Van Kien

Showing results (1-10 of 15) with videos related to

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American Journal of Medical Genetics|September 17, 1998
Vitamin K deficiency embryopathyP Khau Van Kien, A Nivelon-Chevallier, G Spagnolo, et al.
Presse Medicale (Paris, France : 1983)|March 1, 2003
[Late diagnosis of a Di George syndrome]P Manckoundia, P Khau Van Kien, J M Petit, et al.
Journal of Medical Genetics|June 14, 2001
Maternally inherited duplication of the possible imprinted 14q31 regionC Mignon-Ravix, F Mugneret, C Stavropoulou, et al.
American Journal of Medical Genetics|December 14, 1999
Can Hutchinson-Gilford progeria syndrome be a neonatal condition?L Faivre, P Khau Van Kien, N Madinier-Chappat, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|July 17, 2017
[Contribution of chromosomal microarray analysis by a multidisciplinary prenatal diagnosis center]C Bartholmot, E Mousty, F Grosjean, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegalyC Robinet, S Douvier, P Khau Van Kien, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|October 9, 2012
[Pregnancy and Ehlers-Danlos vascular syndrome: patients' care and complications]E Dubruc, S Dupuis-Girod, P Khau Van Kien, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 31, 2008
Compliance and pulse wave velocity assessed by MRI detect early aortic impairment in young patients with mutation of the smooth muscle myosin heavy chainA Lalande, P Khau Van Kien, P M Walker, et al.
International Journal of Oral and Maxillofacial Surgery|February 11, 2010
Extreme oral manifestations in a Marfan-type syndromeR H Khonsari, P Corre, Z Boukerma-Vernex, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|September 17, 1998
Vitamin K deficiency embryopathyP Khau Van Kien, A Nivelon-Chevallier, G Spagnolo, et al.
Presse Medicale (Paris, France : 1983)|March 1, 2003
[Late diagnosis of a Di George syndrome]P Manckoundia, P Khau Van Kien, J M Petit, et al.
Journal of Medical Genetics|June 14, 2001
Maternally inherited duplication of the possible imprinted 14q31 regionC Mignon-Ravix, F Mugneret, C Stavropoulou, et al.
American Journal of Medical Genetics|December 14, 1999
Can Hutchinson-Gilford progeria syndrome be a neonatal condition?L Faivre, P Khau Van Kien, N Madinier-Chappat, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|July 17, 2017
[Contribution of chromosomal microarray analysis by a multidisciplinary prenatal diagnosis center]C Bartholmot, E Mousty, F Grosjean, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegalyC Robinet, S Douvier, P Khau Van Kien, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|October 9, 2012
[Pregnancy and Ehlers-Danlos vascular syndrome: patients' care and complications]E Dubruc, S Dupuis-Girod, P Khau Van Kien, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 31, 2008
Compliance and pulse wave velocity assessed by MRI detect early aortic impairment in young patients with mutation of the smooth muscle myosin heavy chainA Lalande, P Khau Van Kien, P M Walker, et al.
International Journal of Oral and Maxillofacial Surgery|February 11, 2010
Extreme oral manifestations in a Marfan-type syndromeR H Khonsari, P Corre, Z Boukerma-Vernex, et al.
Pageof 2