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L P Ten Kate

Showing results (91-100 of 130) with videos related to

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International Journal of Epidemiology|December 1, 1978
Should we screen all newborns for cystic fibrosis?L P Ten Kate, I Feenstra-de Gooyer, G Ploeg-de Groot, et al.
European Journal of Pediatrics|November 1, 1985
The spectrum of splenogonadal fusion. Case report and review of 84 reported casesA S Gouw, J D Elema, M T Bink-Boelkens, et al.
Lancet (London, England)|September 24, 1988
Prenatal diagnosis of cystic fibrosis where single affected child has diedG I te Meerman, L P ten Kate, J M Cobben, et al.
Human Genetics|July 1, 1996
Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in The NetherlandsH G de Vries, K Niezen-Koning, J W Kliphuis, et al.
American Journal of Medical Genetics|August 1, 1989
Poland anomaly in mother and daughterJ M Cobben, P H Robinson, A J van Essen, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 12, 1998
[Preconception screening of parents and carrier state of cystic fibrosis in the Netherlands: expenses and savings]J B Verheij, H B Hilderink, J G Verzijl, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 1991
[Prevalence at birth of more than 30 congenital disorders in Northern Netherlands]M C Cornel, H E de Walle, T M Haveman, et al.
Lancet (London, England)|October 9, 1993
Allele sharing on chromosome 11q13 in sibs with asthma and atopyJ M Collée, L P ten Kate, H G de Vries, et al.
Human Heredity|January 1, 1996
Comparison of single-entry and double-entry two-step couple screening for cystic fibrosis carriersL P ten Kate, J B Verheij, M F Wildhagen, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibriumH Scheffer, D J Bruinvels, G J te Meerman, et al.
Pageof 13

Showing results (91-100 of 130) with videos related to

Sort By:
Pageof 13
International Journal of Epidemiology|December 1, 1978
Should we screen all newborns for cystic fibrosis?L P Ten Kate, I Feenstra-de Gooyer, G Ploeg-de Groot, et al.
European Journal of Pediatrics|November 1, 1985
The spectrum of splenogonadal fusion. Case report and review of 84 reported casesA S Gouw, J D Elema, M T Bink-Boelkens, et al.
Lancet (London, England)|September 24, 1988
Prenatal diagnosis of cystic fibrosis where single affected child has diedG I te Meerman, L P ten Kate, J M Cobben, et al.
Human Genetics|July 1, 1996
Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in The NetherlandsH G de Vries, K Niezen-Koning, J W Kliphuis, et al.
American Journal of Medical Genetics|August 1, 1989
Poland anomaly in mother and daughterJ M Cobben, P H Robinson, A J van Essen, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 12, 1998
[Preconception screening of parents and carrier state of cystic fibrosis in the Netherlands: expenses and savings]J B Verheij, H B Hilderink, J G Verzijl, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 1991
[Prevalence at birth of more than 30 congenital disorders in Northern Netherlands]M C Cornel, H E de Walle, T M Haveman, et al.
Lancet (London, England)|October 9, 1993
Allele sharing on chromosome 11q13 in sibs with asthma and atopyJ M Collée, L P ten Kate, H G de Vries, et al.
Human Heredity|January 1, 1996
Comparison of single-entry and double-entry two-step couple screening for cystic fibrosis carriersL P ten Kate, J B Verheij, M F Wildhagen, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibriumH Scheffer, D J Bruinvels, G J te Meerman, et al.
Pageof 13