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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 insipidus
A E Meinders, J B Bijlsma
International Archives of Occupational and Environmental Health
|
December 15, 1976
Cytogenetic investigations in volunteers ingesting inorganic lead
J 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 literature
R 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 literature
H W ter Berg, J B Bijlsma, J Willemse
Helvetica Paediatrica Acta
|
July 1, 1972
C8 trisomy mosaicism syndrome
J 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 720D
H F de France, J B Bijlsma, C P Bond
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of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 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 insipidus
A E Meinders, J B Bijlsma
International Archives of Occupational and Environmental Health
|
December 15, 1976
Cytogenetic investigations in volunteers ingesting inorganic lead
J 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 literature
R 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 literature
H W ter Berg, J B Bijlsma, J Willemse
Helvetica Paediatrica Acta
|
July 1, 1972
C8 trisomy mosaicism syndrome
J 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 720D
H F de France, J B Bijlsma, C P Bond
Page
of 4