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Orvosi Hetilap
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September 28, 2000
[22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot]
E Morava, G Masszi, M Czakó, et al.
Central European Journal of Public Health
|
June 17, 2000
Health risk factors and mortality in Pécs City, Hungary in the 1990s
E Morava, E Végh, I Bóna, et al.
Orvosi Hetilap
|
August 3, 2001
[Vascular diseases, spina bifida and schizophrenia in a single family associated with the heterozygote mutation of the heat-sensitive variant of methylenetetrahydrofolate reductase]
A Horváth, E Morava, G Tóth, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Orvosi Hetilap
|
January 23, 1999
[Molecular biologic screening test (PCR) for fragile X syndrome]
E Kovács, E Morava, E Nádasi, et al.
Balkan Journal of Medical Genetics : BJMG
|
January 17, 2020
Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia
J Paprocka, B Rzepka-Migut, N Rzepka, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2007
Distal joint contractures, mental retardation, characteristic face and growth retardation: Chitayat syndrome revisited
S B Wortmann, R Rodenburg, B Schwahn, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2003
A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion
E Morava, O Bartsch, M Czako, et al.
Molecular Genetics and Metabolism
|
September 26, 2013
Abnormal fat distribution in PMM2-CDG
D F G J Wolthuis, E V van Asbeck, T Kozicz, et al.
Journal of Inherited Metabolic Disease
|
December 3, 2011
Glycosylation defects underlying fetal alcohol spectrum disorder: a novel pathogenetic model. "When the wine goes in, strange things come out" - S.T. Coleridge, The Piccolomini
M Binkhorst, S B Wortmann, S Funke, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 96) with videos related to
Sort By:
Page
of 10
Orvosi Hetilap
|
September 28, 2000
[22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot]
E Morava, G Masszi, M Czakó, et al.
Central European Journal of Public Health
|
June 17, 2000
Health risk factors and mortality in Pécs City, Hungary in the 1990s
E Morava, E Végh, I Bóna, et al.
Orvosi Hetilap
|
August 3, 2001
[Vascular diseases, spina bifida and schizophrenia in a single family associated with the heterozygote mutation of the heat-sensitive variant of methylenetetrahydrofolate reductase]
A Horváth, E Morava, G Tóth, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Orvosi Hetilap
|
January 23, 1999
[Molecular biologic screening test (PCR) for fragile X syndrome]
E Kovács, E Morava, E Nádasi, et al.
Balkan Journal of Medical Genetics : BJMG
|
January 17, 2020
Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia
J Paprocka, B Rzepka-Migut, N Rzepka, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 23, 2007
Distal joint contractures, mental retardation, characteristic face and growth retardation: Chitayat syndrome revisited
S B Wortmann, R Rodenburg, B Schwahn, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 28, 2003
A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion
E Morava, O Bartsch, M Czako, et al.
Molecular Genetics and Metabolism
|
September 26, 2013
Abnormal fat distribution in PMM2-CDG
D F G J Wolthuis, E V van Asbeck, T Kozicz, et al.
Journal of Inherited Metabolic Disease
|
December 3, 2011
Glycosylation defects underlying fetal alcohol spectrum disorder: a novel pathogenetic model. "When the wine goes in, strange things come out" - S.T. Coleridge, The Piccolomini
M Binkhorst, S B Wortmann, S Funke, et al.
Page
of 10