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E Legius

Showing results (71-80 of 120) with videos related to

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Clinical and Experimental Immunology|September 1, 1994
Possible association of CD3 and CD4 polymorphisms with insulin-dependent diabetes mellitus (IDDM)M Z Ghabanbasani, I Buyse, E Legius, et al.
Clinical Genetics|April 1, 1996
De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopeniaE Legius, I Wlodarska, L Selleri, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
American Journal of Medical Genetics|May 22, 1995
Diaphragmatic hernia in Denys-Drash syndromeK Devriendt, E Deloof, P Moerman, et al.
Genes, Chromosomes & Cancer|August 1, 1994
TP53 mutations are frequent in malignant NF1 tumorsE Legius, H Dierick, R Wu, et al.
Clinical Genetics|October 8, 2016
Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?C Cassiman, I Casteels, J Jacob, et al.
European Journal of Human Genetics : EJHG|December 18, 2003
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in FlandersAnnick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, et al.
Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.
Journal of Medical Genetics|July 1, 1995
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSASJ C Ruiz, H Cuppens, E Legius, et al.
Prenatal Diagnosis|January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)Ingrid Witters, K Devriendt, E Legius, et al.
Pageof 12

Showing results (71-80 of 120) with videos related to

Sort By:
Pageof 12
Clinical and Experimental Immunology|September 1, 1994
Possible association of CD3 and CD4 polymorphisms with insulin-dependent diabetes mellitus (IDDM)M Z Ghabanbasani, I Buyse, E Legius, et al.
Clinical Genetics|April 1, 1996
De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopeniaE Legius, I Wlodarska, L Selleri, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
American Journal of Medical Genetics|May 22, 1995
Diaphragmatic hernia in Denys-Drash syndromeK Devriendt, E Deloof, P Moerman, et al.
Genes, Chromosomes & Cancer|August 1, 1994
TP53 mutations are frequent in malignant NF1 tumorsE Legius, H Dierick, R Wu, et al.
Clinical Genetics|October 8, 2016
Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?C Cassiman, I Casteels, J Jacob, et al.
European Journal of Human Genetics : EJHG|December 18, 2003
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in FlandersAnnick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, et al.
Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.
Journal of Medical Genetics|July 1, 1995
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSASJ C Ruiz, H Cuppens, E Legius, et al.
Prenatal Diagnosis|January 26, 2002
Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)Ingrid Witters, K Devriendt, E Legius, et al.
Pageof 12