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C Verellen

Showing results (51-60 of 77) with videos related to

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Psychopharmacology|May 5, 1998
Physostigmine results in an increased decrement in brain glucose consumption in Alzheimer's diseaseJ Blin, A Ivanoiu, A De Volder, et al.
Journal De Genetique Humaine|September 1, 1985
[S-100 protein in amniotic fluid of the ancencephalic fetus]M Freund, C J Sindic, N Van Regemorter, et al.
Human Genetics|January 1, 1984
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosomeC Verellen-Dumoulin, M Freund, R De Meyer, et al.
Cancer Genetics and Cytogenetics|January 20, 2000
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;22;21)(q34;q11;q22)B Guillaume, G Ameye, J M Libouton, et al.
Human Mutation|April 27, 2004
Allelic heterogeneity of SMARD1 at the IGHMBP2 locusI Maystadt, M Zarhrate, P Landrieu, et al.
Acta Gastro-Enterologica Belgica|March 1, 1995
The clinical [corrected] background of familial adenomatous polyposis. History, epidemiology, diagnosis and treatmentA Kartheuser, R Detry, S West, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patientM C Belpaire-Dethiou, K Saito, Y Fukuyama, et al.
American Journal of Human Genetics|December 1, 1992
No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21C Pangalos, D Théophile, P M Sinet, et al.
Journal of Medical Genetics|June 9, 2009
17q21.31 microduplication patients are characterised by behavioural problems and poor social interactionB Grisart, L Willatt, A Destrée, et al.
Nature Genetics|September 1, 1994
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndromeT Mochizuki, H H Lemmink, M Mariyama, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Psychopharmacology|May 5, 1998
Physostigmine results in an increased decrement in brain glucose consumption in Alzheimer's diseaseJ Blin, A Ivanoiu, A De Volder, et al.
Journal De Genetique Humaine|September 1, 1985
[S-100 protein in amniotic fluid of the ancencephalic fetus]M Freund, C J Sindic, N Van Regemorter, et al.
Human Genetics|January 1, 1984
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosomeC Verellen-Dumoulin, M Freund, R De Meyer, et al.
Cancer Genetics and Cytogenetics|January 20, 2000
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;22;21)(q34;q11;q22)B Guillaume, G Ameye, J M Libouton, et al.
Human Mutation|April 27, 2004
Allelic heterogeneity of SMARD1 at the IGHMBP2 locusI Maystadt, M Zarhrate, P Landrieu, et al.
Acta Gastro-Enterologica Belgica|March 1, 1995
The clinical [corrected] background of familial adenomatous polyposis. History, epidemiology, diagnosis and treatmentA Kartheuser, R Detry, S West, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patientM C Belpaire-Dethiou, K Saito, Y Fukuyama, et al.
American Journal of Human Genetics|December 1, 1992
No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21C Pangalos, D Théophile, P M Sinet, et al.
Journal of Medical Genetics|June 9, 2009
17q21.31 microduplication patients are characterised by behavioural problems and poor social interactionB Grisart, L Willatt, A Destrée, et al.
Nature Genetics|September 1, 1994
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndromeT Mochizuki, H H Lemmink, M Mariyama, et al.
Pageof 8