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E Vamos

Showing results (101-110 of 129) with videos related to

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American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblastsN Telerman-Toppet, D Biarent, J M Bouton, et al.
Fetal Diagnosis and Therapy|May 1, 1995
Cordocentesis for rapid karyotype: 421 consecutive casesC Donner, F Rypens, V Paquet, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Prenatal diagnosis of malformations of the central nervous system]N Elkhazen, J Dodion, E Vamos, et al.
Acta Clinica Belgica|January 1, 1996
Hyperphosphatasemia in early diagnosed infantile GM1 gangliosidosis presenting as transient hydrops fetalisR Denis, J L Wayenberg, M Vermeulen, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis and confirmation of infantile sialic acid storage diseaseE Vamos, J Libert, N Elkhazen, et al.
Molecular Human Reproduction|December 2, 2000
Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiencyK Sermon, P Henderix, W Lissens, et al.
Revue Medicale De Bruxelles|June 1, 1984
[Prenatal diagnosis of malformations of the central nervous system]N el Khazen, J Dodion, E Vamos, et al.
The Journal of Clinical Investigation|July 1, 1994
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitusM J Abramowicz, M Andrien, E Dupont, et al.
American Journal of Medical Genetics|May 30, 1998
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactylyW Courtens, W Tjalma, L Messiaen, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|April 10, 1995
Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalitiesG Pierquin, P Peeters, F Roels, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblastsN Telerman-Toppet, D Biarent, J M Bouton, et al.
Fetal Diagnosis and Therapy|May 1, 1995
Cordocentesis for rapid karyotype: 421 consecutive casesC Donner, F Rypens, V Paquet, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Prenatal diagnosis of malformations of the central nervous system]N Elkhazen, J Dodion, E Vamos, et al.
Acta Clinica Belgica|January 1, 1996
Hyperphosphatasemia in early diagnosed infantile GM1 gangliosidosis presenting as transient hydrops fetalisR Denis, J L Wayenberg, M Vermeulen, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis and confirmation of infantile sialic acid storage diseaseE Vamos, J Libert, N Elkhazen, et al.
Molecular Human Reproduction|December 2, 2000
Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiencyK Sermon, P Henderix, W Lissens, et al.
Revue Medicale De Bruxelles|June 1, 1984
[Prenatal diagnosis of malformations of the central nervous system]N el Khazen, J Dodion, E Vamos, et al.
The Journal of Clinical Investigation|July 1, 1994
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitusM J Abramowicz, M Andrien, E Dupont, et al.
American Journal of Medical Genetics|May 30, 1998
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactylyW Courtens, W Tjalma, L Messiaen, et al.
Pageof 13