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C B van der Hagen

Showing results (1-10 of 16) with videos related to

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American Journal of Medical Genetics|September 15, 1992
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)N Tommerup, C B van der Hagen, A Heiberg
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 10, 1994
[Genetic disease in general practice. An interview study among general practitioners in Oppland and Oslo]E Hem, C B van der Hagen, M H Solaas
Clinical Genetics|March 1, 1975
Polycythemia vera treated with -32p and myleran: development of chronic granulocytic leukemia with chromosomal abnormalities in one patientP Staven, C B VAN DER Hagen, E Vogt, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 10, 1989
[Cytogenetic analysis in acute leukemia]L Brinch, S A Evensen, P Stavem, et al.
European Journal of Pediatrics|April 1, 1993
Campomelic dysplasia--an underdiagnosed condition?E K Normann, J C Pedersen, G Stiris, et al.
Journal of Medical Genetics|July 1, 1994
Instability of lymphocyte chromosomes in a girl with Rothmund-Thomson syndromeK H Orstavik, N McFadden, J Hagelsteen, et al.
Clinical Genetics|June 1, 1985
Deficiency of fumarylacetoacetase without hereditary tyrosinemiaE A Kvittingen, A L Børresen, O Stokke, et al.
Journal of Medical Genetics|July 15, 2005
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 1990
[Prenatal ultrasonic diagnosis and Down's syndrome]K A Salvesen, S H Eik-Nes, J M Tuveng, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 21, 2000
A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotypeC V Isaksen, S H Eik-Nes, H G Blaas, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|September 15, 1992
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)N Tommerup, C B van der Hagen, A Heiberg
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 10, 1994
[Genetic disease in general practice. An interview study among general practitioners in Oppland and Oslo]E Hem, C B van der Hagen, M H Solaas
Clinical Genetics|March 1, 1975
Polycythemia vera treated with -32p and myleran: development of chronic granulocytic leukemia with chromosomal abnormalities in one patientP Staven, C B VAN DER Hagen, E Vogt, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 10, 1989
[Cytogenetic analysis in acute leukemia]L Brinch, S A Evensen, P Stavem, et al.
European Journal of Pediatrics|April 1, 1993
Campomelic dysplasia--an underdiagnosed condition?E K Normann, J C Pedersen, G Stiris, et al.
Journal of Medical Genetics|July 1, 1994
Instability of lymphocyte chromosomes in a girl with Rothmund-Thomson syndromeK H Orstavik, N McFadden, J Hagelsteen, et al.
Clinical Genetics|June 1, 1985
Deficiency of fumarylacetoacetase without hereditary tyrosinemiaE A Kvittingen, A L Børresen, O Stokke, et al.
Journal of Medical Genetics|July 15, 2005
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 1990
[Prenatal ultrasonic diagnosis and Down's syndrome]K A Salvesen, S H Eik-Nes, J M Tuveng, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 21, 2000
A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotypeC V Isaksen, S H Eik-Nes, H G Blaas, et al.
Pageof 2