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L P ten Kate

Showing results (41-50 of 130) with videos related to

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Lancet (London, England)|December 3, 1988
Prenatal diagnosis of cystic fibrosisG J te Meerman, L P ten Kate, C C Buys
Humangenetik|March 23, 1973
Serum dependency of cellular phenotype in mucopolysaccharidoses: the influence of autologous serum on metachromasiaL P ten Kate, G J Anders, C J de Groot
Tijdschrift Voor Kindergeneeskunde|February 1, 1993
[Complete situs inversus in one half of monozygotic twins]L P ten Kate, A J van Essen, M C Cornel
Teratology|September 1, 1990
Association between ovulation stimulation, in vitro fertilisation, and neural tube defects?M C Cornel, L P ten Kate, G J te Meerman
American Journal of Human Genetics|June 1, 1986
On the power to detect differences between male and female mutation rates for Duchenne muscular dystrophy, using classical segregation analysis and restriction fragment length polymorphismsE R Karel, G J te Meerman, L P Ten Kate
Lancet (London, England)|December 23, 1989
Ovulation induction, in-vitro fertilisation, and neural tube defectsM C Cornel, L P Ten Kate, G J Te Meerman
The American Journal of Cardiology|November 1, 1982
Familial aggregation of coronary heart disease and its relation to known genetic risk factorsL P ten Kate, H Boman, S P Daiger, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Humangenetik|January 1, 1973
A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding techniqueW L Gouw, L P ten Kate, G J Anders, et al.
American Journal of Medical Genetics|July 1, 1990
Prevalence of lethal osteochondrodysplasiasJ M Cobben, M C Cornel, I Dijkstra, et al.
Pageof 13

Showing results (41-50 of 130) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|December 3, 1988
Prenatal diagnosis of cystic fibrosisG J te Meerman, L P ten Kate, C C Buys
Humangenetik|March 23, 1973
Serum dependency of cellular phenotype in mucopolysaccharidoses: the influence of autologous serum on metachromasiaL P ten Kate, G J Anders, C J de Groot
Tijdschrift Voor Kindergeneeskunde|February 1, 1993
[Complete situs inversus in one half of monozygotic twins]L P ten Kate, A J van Essen, M C Cornel
Teratology|September 1, 1990
Association between ovulation stimulation, in vitro fertilisation, and neural tube defects?M C Cornel, L P ten Kate, G J te Meerman
American Journal of Human Genetics|June 1, 1986
On the power to detect differences between male and female mutation rates for Duchenne muscular dystrophy, using classical segregation analysis and restriction fragment length polymorphismsE R Karel, G J te Meerman, L P Ten Kate
Lancet (London, England)|December 23, 1989
Ovulation induction, in-vitro fertilisation, and neural tube defectsM C Cornel, L P Ten Kate, G J Te Meerman
The American Journal of Cardiology|November 1, 1982
Familial aggregation of coronary heart disease and its relation to known genetic risk factorsL P ten Kate, H Boman, S P Daiger, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 1990
[Carrier detection in relatives of patients with cystic fibrosis and their partners]L P ten Kate, H Scheffer, D J Halley, et al.
Humangenetik|January 1, 1973
A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding techniqueW L Gouw, L P ten Kate, G J Anders, et al.
American Journal of Medical Genetics|July 1, 1990
Prevalence of lethal osteochondrodysplasiasJ M Cobben, M C Cornel, I Dijkstra, et al.
Pageof 13