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Placenta
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July 1, 1987
Placental electron microscopy and histochemistry in a case of sialic acid storage disorder
E Jauniaux, E Vamos, J Libert, et al.
Lancet (London, England)
|
January 23, 1993
In-utero carbon monoxide poisoning and multiple fetal abnormalities
Y Hennequin, D Blum, E Vamos, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluid
A Kumps, E Vamos, Y Mardens, et al.
The Journal of Pediatrics
|
January 1, 1992
Hyperphosphatasemia in GM1 gangliosidosis
R Denis, J L Wayemberg, M Vermeulen, et al.
Acta Paediatrica Belgica
|
April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosis
N Van Regemorter, J Dodion, C Druart, et al.
Bruxelles Medical
|
October 1, 1974
[Antenatal diagnosis of congenital diseases: indications, limitations, and technic]
E Vamos-Hurwitz, P Petit, M Mathy, et al.
Acta Paediatrica Scandinavica
|
January 1, 1978
Farber's disease as a ceramidosis: clinical, radiological and biochemical aspects
M Toppet, E Vamos-Hurwitz, G Jonniaux, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1993
Chromosomal findings in cultured melanocytes from a giant congenital nevus
P Heimann, G Ogur, C De Busscher, et al.
Acta Paediatrica Belgica
|
April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case
M Tondeur, E Vamos-Hurwitz, M Cantz, et al.
Acta Paediatrica Scandinavica
|
November 1, 1975
Mannosidosis: findings in cultured fibroblasts and urine
E Vamos-Hurwitz, M Tondeur, R Humbel, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 129) with videos related to
Sort By:
Page
of 13
Placenta
|
July 1, 1987
Placental electron microscopy and histochemistry in a case of sialic acid storage disorder
E Jauniaux, E Vamos, J Libert, et al.
Lancet (London, England)
|
January 23, 1993
In-utero carbon monoxide poisoning and multiple fetal abnormalities
Y Hennequin, D Blum, E Vamos, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluid
A Kumps, E Vamos, Y Mardens, et al.
The Journal of Pediatrics
|
January 1, 1992
Hyperphosphatasemia in GM1 gangliosidosis
R Denis, J L Wayemberg, M Vermeulen, et al.
Acta Paediatrica Belgica
|
April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosis
N Van Regemorter, J Dodion, C Druart, et al.
Bruxelles Medical
|
October 1, 1974
[Antenatal diagnosis of congenital diseases: indications, limitations, and technic]
E Vamos-Hurwitz, P Petit, M Mathy, et al.
Acta Paediatrica Scandinavica
|
January 1, 1978
Farber's disease as a ceramidosis: clinical, radiological and biochemical aspects
M Toppet, E Vamos-Hurwitz, G Jonniaux, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1993
Chromosomal findings in cultured melanocytes from a giant congenital nevus
P Heimann, G Ogur, C De Busscher, et al.
Acta Paediatrica Belgica
|
April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case
M Tondeur, E Vamos-Hurwitz, M Cantz, et al.
Acta Paediatrica Scandinavica
|
November 1, 1975
Mannosidosis: findings in cultured fibroblasts and urine
E Vamos-Hurwitz, M Tondeur, R Humbel, et al.
Page
of 13