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J B Bijlsma

Showing results (1-10 of 38) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|May 9, 1981
[A patient with ring chromosome 13]A Hammond, J B Bijlsma
Folia Medica Neerlandica|January 1, 1970
A family with congenital hypothalamic neurohypophyseal diabetes insipidusA E Meinders, J B Bijlsma
International Archives of Occupational and Environmental Health|December 15, 1976
Cytogenetic investigations in volunteers ingesting inorganic leadJ B Bijlsma, H F de France
American Journal of Medical Genetics|September 1, 1987
Further delineation of the 3-M syndrome with review of the literatureR C Hennekam, J B Bijlsma, J Spranger
Tijdschrift Voor Kindergeneeskunde|December 1, 1987
[Prognosis in the cri-du-chat syndrome]J C Oosterwijk, A J Verboom, J B Bijlsma
Neuropediatrics|November 1, 1987
Familial occurrence of intracranial aneurysms in childhood: a case report and review of the literatureH W ter Berg, J B Bijlsma, J Willemse
Helvetica Paediatrica Acta|July 1, 1972
C8 trisomy mosaicism syndromeJ B Bijlsma, J C Wijffels, W H Tegelaers
Humangenetik|January 1, 1971
Duplication deficiency syndrome in familial translocation (2q-;5p+)J B Bijlsma, H de France, E M Bleeker-Wagemakers
Human Genetics|August 31, 1977
Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?M H Breuning, J B Bijlsma, H F de France
Humangenetik|May 17, 1974
Direct Giemsa-banding pattern analysis of human chromosomes by means of a television microdensitometer: the Quantimet 720DH F de France, J B Bijlsma, C P Bond
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Nederlands Tijdschrift Voor Geneeskunde|May 9, 1981
[A patient with ring chromosome 13]A Hammond, J B Bijlsma
Folia Medica Neerlandica|January 1, 1970
A family with congenital hypothalamic neurohypophyseal diabetes insipidusA E Meinders, J B Bijlsma
International Archives of Occupational and Environmental Health|December 15, 1976
Cytogenetic investigations in volunteers ingesting inorganic leadJ B Bijlsma, H F de France
American Journal of Medical Genetics|September 1, 1987
Further delineation of the 3-M syndrome with review of the literatureR C Hennekam, J B Bijlsma, J Spranger
Tijdschrift Voor Kindergeneeskunde|December 1, 1987
[Prognosis in the cri-du-chat syndrome]J C Oosterwijk, A J Verboom, J B Bijlsma
Neuropediatrics|November 1, 1987
Familial occurrence of intracranial aneurysms in childhood: a case report and review of the literatureH W ter Berg, J B Bijlsma, J Willemse
Helvetica Paediatrica Acta|July 1, 1972
C8 trisomy mosaicism syndromeJ B Bijlsma, J C Wijffels, W H Tegelaers
Humangenetik|January 1, 1971
Duplication deficiency syndrome in familial translocation (2q-;5p+)J B Bijlsma, H de France, E M Bleeker-Wagemakers
Human Genetics|August 31, 1977
Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?M H Breuning, J B Bijlsma, H F de France
Humangenetik|May 17, 1974
Direct Giemsa-banding pattern analysis of human chromosomes by means of a television microdensitometer: the Quantimet 720DH F de France, J B Bijlsma, C P Bond
Pageof 4