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American Journal of Medical Genetics
|
March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneity
C Schrander-Stumpel, J P Fryns, F A Beemer, et al.
Journal of Medical Genetics
|
March 8, 2003
Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hips
G R Mortier, P P G Kramer, A Giedion, et al.
Clinical Genetics
|
April 29, 1998
VSD, hypospadias and normal psychomotor development in a patient with inv dup 8(q13-q21.2)
J C Giltay, J A Bokma, H de France, et al.
Archives of Physical Medicine and Rehabilitation
|
December 23, 1998
Osteogenesis imperfecta in childhood: treatment strategies
R H Engelbert, H E Pruijs, F A Beemer, et al.
Nederlands Tijdschrift Voor Tandheelkunde
|
November 1, 1990
[Oligodontia]
Y van der Weide, W H Steen, F A Beemer, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 22, 1995
[Incidence and prevalence of hemoglobinopathies in children in The Netherlands]
J H Rengelink-van der Lee, T W Schulpen, F A Beemer
Tijdschrift Voor Kindergeneeskunde
|
June 1, 1983
[Thoracic pelvic phalangeal dystrophy (Jeune's syndrome)]
R C Hennekam, F A Beemer, L J Gerards, et al.
Pediatric Research
|
May 1, 1987
D-glyceric acidemia: an inborn error associated with fructose metabolism
M Duran, F A Beemer, L Bruinvis, et al.
Clinical Genetics
|
May 1, 1985
Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43)
F A Beemer, J M Klep-de Pater, G J Sepers, et al.
European Journal of Pediatrics
|
April 1, 1986
The Aase syndrome. Case report and review of the literature
N Muis, F A Beemer, P van Dijken, et al.
Page
of 18
Search research articles
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Showing results (41-50 of 177) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics
|
March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneity
C Schrander-Stumpel, J P Fryns, F A Beemer, et al.
Journal of Medical Genetics
|
March 8, 2003
Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hips
G R Mortier, P P G Kramer, A Giedion, et al.
Clinical Genetics
|
April 29, 1998
VSD, hypospadias and normal psychomotor development in a patient with inv dup 8(q13-q21.2)
J C Giltay, J A Bokma, H de France, et al.
Archives of Physical Medicine and Rehabilitation
|
December 23, 1998
Osteogenesis imperfecta in childhood: treatment strategies
R H Engelbert, H E Pruijs, F A Beemer, et al.
Nederlands Tijdschrift Voor Tandheelkunde
|
November 1, 1990
[Oligodontia]
Y van der Weide, W H Steen, F A Beemer, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 22, 1995
[Incidence and prevalence of hemoglobinopathies in children in The Netherlands]
J H Rengelink-van der Lee, T W Schulpen, F A Beemer
Tijdschrift Voor Kindergeneeskunde
|
June 1, 1983
[Thoracic pelvic phalangeal dystrophy (Jeune's syndrome)]
R C Hennekam, F A Beemer, L J Gerards, et al.
Pediatric Research
|
May 1, 1987
D-glyceric acidemia: an inborn error associated with fructose metabolism
M Duran, F A Beemer, L Bruinvis, et al.
Clinical Genetics
|
May 1, 1985
Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43)
F A Beemer, J M Klep-de Pater, G J Sepers, et al.
European Journal of Pediatrics
|
April 1, 1986
The Aase syndrome. Case report and review of the literature
N Muis, F A Beemer, P van Dijken, et al.
Page
of 18