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E Vamos

Showing results (111-120 of 129) with videos related to

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Cancer Genetics and Cytogenetics|July 1, 1996
Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcomaG Oğur, Z Sengun, G Arel-Kiliç, et al.
Revue Medicale De Bruxelles|June 1, 1990
[Cordocentesis: experience in 391 initial samples]C Donner, P Simon, F Gosselin, et al.
Oncogene|July 20, 1995
Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancerK Amfo, B Neyns, E Teugels, et al.
Archives Francaises De Pediatrie|October 1, 1972
[Mucolipidosis of type II (I-cell disease): study of 3 cases]R Walbaum, P Dehaene, W Scharfman, et al.
Archives Francaises De Pediatrie|June 1, 1973
[Type II mucolipidosis (I-cell disease)]R Walbaum, P Dehaene, W Scharfman, et al.
Diabetologia|April 1, 1993
Congenital absence of insulin cells in a neonate with diabetes mellitus and mutase-deficient methylmalonic acidaemiaD Blum, H Dorchy, T Mouraux, et al.
Pediatric Neurology|May 1, 1993
Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosisL De Meirleir, W Lissens, R Denis, et al.
European Journal of Pediatrics|February 7, 1998
Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiencyL H Cohen, E Vamos, C Heinrichs, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcomeN Van Regemorter, E Vamos, V Defleur, et al.
Revue Medicale De Bruxelles|February 15, 2003
[Medical genetics service]G Vassart, M Abramowicz, P Cochaux, et al.
Pageof 13

Showing results (111-120 of 129) with videos related to

Sort By:
Pageof 13
Cancer Genetics and Cytogenetics|July 1, 1996
Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcomaG Oğur, Z Sengun, G Arel-Kiliç, et al.
Revue Medicale De Bruxelles|June 1, 1990
[Cordocentesis: experience in 391 initial samples]C Donner, P Simon, F Gosselin, et al.
Oncogene|July 20, 1995
Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancerK Amfo, B Neyns, E Teugels, et al.
Archives Francaises De Pediatrie|October 1, 1972
[Mucolipidosis of type II (I-cell disease): study of 3 cases]R Walbaum, P Dehaene, W Scharfman, et al.
Archives Francaises De Pediatrie|June 1, 1973
[Type II mucolipidosis (I-cell disease)]R Walbaum, P Dehaene, W Scharfman, et al.
Diabetologia|April 1, 1993
Congenital absence of insulin cells in a neonate with diabetes mellitus and mutase-deficient methylmalonic acidaemiaD Blum, H Dorchy, T Mouraux, et al.
Pediatric Neurology|May 1, 1993
Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosisL De Meirleir, W Lissens, R Denis, et al.
European Journal of Pediatrics|February 7, 1998
Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiencyL H Cohen, E Vamos, C Heinrichs, et al.
Acta Obstetricia Et Gynecologica Scandinavica|January 1, 1986
Pathological pregnancies. Results of amniotic fluid studies and fetal outcomeN Van Regemorter, E Vamos, V Defleur, et al.
Revue Medicale De Bruxelles|February 15, 2003
[Medical genetics service]G Vassart, M Abramowicz, P Cochaux, et al.
Pageof 13