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E M Bleeker-Wagemakers

Showing results (1-10 of 67) with videos related to

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Pediatric Radiology|April 10, 1978
Hereditary malformation of the toes and fingers in a family with double translocation heterozygosityP F Dijkstra, E M Bleeker-Wagemakers
American Journal of Medical Genetics|January 1, 1989
A girl with the Pitt-Rogers-Danks syndromeJ W Oorthuys, E M Bleeker-Wagemakers
Ophthalmic Paediatrics and Genetics|November 1, 1988
Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosomeE M Bleeker-Wagemakers, I Zweije-Hofman, A Gal
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1976
Congenital eversion of the eyelids in a case of Down's syndromeE M Bleeker-Wagemakers, J W Delleman, K Walbeek
Ophthalmic Paediatrics and Genetics|September 1, 1993
Mitochondrial DNA analysis as a diagnostic tool in singleton cases of Leber's hereditary optic neuropathyR J Oostra, P A Bolhuis, E M Bleeker-Wagemakers
Humangenetik|January 1, 1971
Duplication deficiency syndrome in familial translocation (2q-;5p+)J B Bijlsma, H de France, E M Bleeker-Wagemakers
Ophthalmic Paediatrics and Genetics|March 1, 1991
Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome)F M Meire, W J Delleman, E M Bleeker-Wagemakers
Nederlands Tijdschrift Voor Geneeskunde|December 5, 1987
[Heredity in ophthalmology]J W Delleman, E M Bleeker-Wagemakers, M J van Schooneveld
Journal of Pediatric Ophthalmology|July 1, 1977
Opacities of the lens indicating carrier status in the oculo-cerebro-renal (Lowe) syndromeJ W Delleman, E M Bleeker-Wagemakers, A W van Veelen
Human Genetics|April 1, 1996
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersR J Oostra, S Kemp, P A Bolhuis, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Pediatric Radiology|April 10, 1978
Hereditary malformation of the toes and fingers in a family with double translocation heterozygosityP F Dijkstra, E M Bleeker-Wagemakers
American Journal of Medical Genetics|January 1, 1989
A girl with the Pitt-Rogers-Danks syndromeJ W Oorthuys, E M Bleeker-Wagemakers
Ophthalmic Paediatrics and Genetics|November 1, 1988
Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosomeE M Bleeker-Wagemakers, I Zweije-Hofman, A Gal
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1976
Congenital eversion of the eyelids in a case of Down's syndromeE M Bleeker-Wagemakers, J W Delleman, K Walbeek
Ophthalmic Paediatrics and Genetics|September 1, 1993
Mitochondrial DNA analysis as a diagnostic tool in singleton cases of Leber's hereditary optic neuropathyR J Oostra, P A Bolhuis, E M Bleeker-Wagemakers
Humangenetik|January 1, 1971
Duplication deficiency syndrome in familial translocation (2q-;5p+)J B Bijlsma, H de France, E M Bleeker-Wagemakers
Ophthalmic Paediatrics and Genetics|March 1, 1991
Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome)F M Meire, W J Delleman, E M Bleeker-Wagemakers
Nederlands Tijdschrift Voor Geneeskunde|December 5, 1987
[Heredity in ophthalmology]J W Delleman, E M Bleeker-Wagemakers, M J van Schooneveld
Journal of Pediatric Ophthalmology|July 1, 1977
Opacities of the lens indicating carrier status in the oculo-cerebro-renal (Lowe) syndromeJ W Delleman, E M Bleeker-Wagemakers, A W van Veelen
Human Genetics|April 1, 1996
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersR J Oostra, S Kemp, P A Bolhuis, et al.
Pageof 7