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Revue Medicale De Bruxelles
|
February 15, 2003
[Medical genetics service]
G Vassart, M Abramowicz, P Cochaux, et al.
Human Genetics
|
September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome
G Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Human Genetics
|
February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1
L Krols, J J Martin, G David, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
March 1, 1993
Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis
L Verstraeten, N Van Regemorter, A Pardou, et al.
Human Genetics
|
March 10, 1999
Delineation of two distinct 6p deletion syndromes
A F Davies, G Mirza, G Sekhon, et al.
Human Genetics
|
October 1, 1996
A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome
A F Davies, M G Olavesen, R J Stephens, et al.
Acta Neuropathologica
|
January 1, 1994
On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family
J J Martin, N Van Regemorter, L Krols, et al.
American Journal of Medical Genetics
|
July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies
W Courtens, M B Petersen, J C Noël, et al.
Nature Genetics
|
February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family
S Abdelhak, V Kalatzis, R Heilig, et al.
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation
Nisha Limaye, N Revencu, N Van Regemorter, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 71) with videos related to
Sort By:
Page
of 8
Revue Medicale De Bruxelles
|
February 15, 2003
[Medical genetics service]
G Vassart, M Abramowicz, P Cochaux, et al.
Human Genetics
|
September 1, 1991
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome
G Pierquin, N Van Regemorter, Hayez-Delatte, et al.
Human Genetics
|
February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1
L Krols, J J Martin, G David, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
March 1, 1993
Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis
L Verstraeten, N Van Regemorter, A Pardou, et al.
Human Genetics
|
March 10, 1999
Delineation of two distinct 6p deletion syndromes
A F Davies, G Mirza, G Sekhon, et al.
Human Genetics
|
October 1, 1996
A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome
A F Davies, M G Olavesen, R J Stephens, et al.
Acta Neuropathologica
|
January 1, 1994
On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family
J J Martin, N Van Regemorter, L Krols, et al.
American Journal of Medical Genetics
|
July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies
W Courtens, M B Petersen, J C Noël, et al.
Nature Genetics
|
February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family
S Abdelhak, V Kalatzis, R Heilig, et al.
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation
Nisha Limaye, N Revencu, N Van Regemorter, et al.
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of 8