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F A Beemer

Showing results (41-50 of 177) with videos related to

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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 heterogeneityC 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 hipsG 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 strategiesR 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 metabolismM 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 literatureN Muis, F A Beemer, P van Dijken, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
American Journal of Medical Genetics|March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneityC 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 hipsG 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 strategiesR 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 metabolismM 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 literatureN Muis, F A Beemer, P van Dijken, et al.
Pageof 18