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Annales De Genetique
|
January 1, 1987
Chromosome 22 mosaic monosomy (46,XY/45,XY,-22)
A Verloes, C Herens, C Lambotte, et al.
American Journal of Medical Genetics
|
July 1, 1987
Noonan and Klinefelter syndromes in a child
A Verloes, O Guidi, J Frederic, et al.
Annales De Genetique
|
August 28, 2001
Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens
A Verloes, M Jamar, V Dideberg, et al.
Acta Chirurgica Belgica
|
November 27, 1998
Pathogenesis of abdominal aortic aneurysm (AAA) formation
R Limet, B Nusgens, A Verloes, et al.
Annals of the New York Academy of Sciences
|
November 18, 1996
Genetic aspects of abdominal aortic aneurysm
A Verloes, N Sakalihasan, R Limet, et al.
Journal of Medical Genetics
|
August 1, 1995
Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands
A Verloes, A David, L Ngô, et al.
American Journal of Medical Genetics
|
November 1, 1989
BBBG syndrome or Opitz syndrome: new family
A Verloes, M Le Merrer, M L Briard
Journal of Vascular Surgery
|
April 1, 1995
Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees
A Verloes, N Sakalihasan, L Koulischer, et al.
Revue Medicale De Liege
|
October 6, 2006
[Tall stature: some classical syndromes]
N Gusbin, A Verloes, A Daly, et al.
Revue Medicale De Liege
|
December 1, 1991
[Prenatal screening for trisomy 21 in maternal blood. Focus]
L Koulischer, R Schoos, A Verloes, et al.
Page
of 21
Search research articles
Search
Showing results (41-50 of 206) with videos related to
Sort By:
Page
of 21
Annales De Genetique
|
January 1, 1987
Chromosome 22 mosaic monosomy (46,XY/45,XY,-22)
A Verloes, C Herens, C Lambotte, et al.
American Journal of Medical Genetics
|
July 1, 1987
Noonan and Klinefelter syndromes in a child
A Verloes, O Guidi, J Frederic, et al.
Annales De Genetique
|
August 28, 2001
Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens
A Verloes, M Jamar, V Dideberg, et al.
Acta Chirurgica Belgica
|
November 27, 1998
Pathogenesis of abdominal aortic aneurysm (AAA) formation
R Limet, B Nusgens, A Verloes, et al.
Annals of the New York Academy of Sciences
|
November 18, 1996
Genetic aspects of abdominal aortic aneurysm
A Verloes, N Sakalihasan, R Limet, et al.
Journal of Medical Genetics
|
August 1, 1995
Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands
A Verloes, A David, L Ngô, et al.
American Journal of Medical Genetics
|
November 1, 1989
BBBG syndrome or Opitz syndrome: new family
A Verloes, M Le Merrer, M L Briard
Journal of Vascular Surgery
|
April 1, 1995
Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees
A Verloes, N Sakalihasan, L Koulischer, et al.
Revue Medicale De Liege
|
October 6, 2006
[Tall stature: some classical syndromes]
N Gusbin, A Verloes, A Daly, et al.
Revue Medicale De Liege
|
December 1, 1991
[Prenatal screening for trisomy 21 in maternal blood. Focus]
L Koulischer, R Schoos, A Verloes, et al.
Page
of 21