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Gynecologie, Obstetrique & Fertilite|September 6, 2005
[Extending preimplantation genetic diagnosis to HLA typing: the Paris experience]J Steffann, N Frydman, P Burlet, et al.American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.Clinical Genetics|March 18, 2004
Novel CFTR mutations in black cystic fibrosis patientsM N Feuillet-Fieux, M Ferrec, N Gigarel, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Prenatal diagnosis of autosomal recessive polycystic kidney disease]M F Gagnadoux, T Attié, J Amiel, et al.Reproductive Biomedicine Online|February 7, 2008
Preimplantation genetic diagnosis for autosomal recessive polycystic kidney diseaseN Gigarel, N Frydman, P Burlet, et al.Prenatal Diagnosis|February 17, 2001
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiencyP F Ray, N Gigarel, J P Bonnefont, et al.Molecular Human Reproduction|August 10, 2006
Multiple displacement amplification improves PGD for fragile X syndromeP Burlet, N Frydman, N Gigarel, et al.American Journal of Human Genetics|October 3, 2000
Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathyI Valnot, S Osmond, N Gigarel, et al.Fetal Diagnosis and Therapy|December 23, 2000
Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biologyD Mahieu-Caputo, P Sonigo, J Amiel, et al.Journal of Medical Genetics|June 5, 2007
Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndromeJ Steffann, N Gigarel, J Corcos, et al.Pageof 2