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Tijdschrift Voor Kindergeneeskunde
|
October 1, 1984
[Monozygotic twins with Williams-Beuren or 'elfen-face' syndrome]
J W Oorthuys
European Journal of Pediatrics
|
September 1, 1979
The Langer-Giedion-syndrome (tricho-rhino-phalangeal syndrome, type II)
J W Oorthuys, F A Beemer
American Journal of Medical Genetics
|
January 1, 1989
A girl with the Pitt-Rogers-Danks syndrome
J W Oorthuys, E M Bleeker-Wagemakers
Tijdschrift Voor Kindergeneeskunde
|
December 1, 1984
[Congenital muscular dystrophy--its spectrum]
P G Barth, P Fleury, J W Oorthuys
European Journal of Pediatrics
|
April 1, 1996
Acromicric dysplasia and geleophysic dysplasia: similarities and differences
R C Hennekam, Y van Bever, J W Oorthuys
Clinical Genetics
|
June 1, 1989
Mosaic 47,XY,+8/48,XXYY in a mentally non-retarded man with phenotypical and neurological abnormalities
J M Hoovers, J W Oorthuys, M de Visser
Journal of Medical Genetics
|
April 1, 1988
De novo partial trisomy 15q (proximal type)
T J Herweijer, J W Oorthuys, N J Leschot
Clinical Genetics
|
August 1, 1981
Partial trisomy 3q due to a de novo translocation t(X;3) (p21;q12)
J W Oorthuys, R M Slater, H Barrowclough, et al.
Archives of Disease in Childhood
|
September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IV
F M Pope, P Narcisi, A C Nicholls, et al.
Clinical Genetics
|
February 1, 1986
Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome
E M Bleeker-Wagemakers, J W Oorthuys, R J Wanders, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Tijdschrift Voor Kindergeneeskunde
|
October 1, 1984
[Monozygotic twins with Williams-Beuren or 'elfen-face' syndrome]
J W Oorthuys
European Journal of Pediatrics
|
September 1, 1979
The Langer-Giedion-syndrome (tricho-rhino-phalangeal syndrome, type II)
J W Oorthuys, F A Beemer
American Journal of Medical Genetics
|
January 1, 1989
A girl with the Pitt-Rogers-Danks syndrome
J W Oorthuys, E M Bleeker-Wagemakers
Tijdschrift Voor Kindergeneeskunde
|
December 1, 1984
[Congenital muscular dystrophy--its spectrum]
P G Barth, P Fleury, J W Oorthuys
European Journal of Pediatrics
|
April 1, 1996
Acromicric dysplasia and geleophysic dysplasia: similarities and differences
R C Hennekam, Y van Bever, J W Oorthuys
Clinical Genetics
|
June 1, 1989
Mosaic 47,XY,+8/48,XXYY in a mentally non-retarded man with phenotypical and neurological abnormalities
J M Hoovers, J W Oorthuys, M de Visser
Journal of Medical Genetics
|
April 1, 1988
De novo partial trisomy 15q (proximal type)
T J Herweijer, J W Oorthuys, N J Leschot
Clinical Genetics
|
August 1, 1981
Partial trisomy 3q due to a de novo translocation t(X;3) (p21;q12)
J W Oorthuys, R M Slater, H Barrowclough, et al.
Archives of Disease in Childhood
|
September 1, 1988
Clinical presentations of Ehlers Danlos syndrome type IV
F M Pope, P Narcisi, A C Nicholls, et al.
Clinical Genetics
|
February 1, 1986
Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome
E M Bleeker-Wagemakers, J W Oorthuys, R J Wanders, et al.
Page
of 3