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A van Haeringen

Showing results (11-20 of 60) with videos related to

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Animal Genetics|November 1, 2011
Population studies of 17 equine STR for forensic and phylogenetic analysisL H P van de Goor, W A van Haeringen, J A Lenstra
Melanoma Research|June 4, 1998
Multiple agminate Spitz naeviM M Hulshof, A van Haeringen, N A Gruis, et al.
American Journal of Medical Genetics|December 2, 1996
Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotypeM C Lindeman-Kusse, A Van Haeringen, J J Hoorweg-Nijman, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 6, 1987
[Familial dysplastic nevus syndrome in the Netherlands; various clinical and genetic aspects]W Bergman, A Palan, A van Haeringen, et al.
European Journal of Cancer & Clinical Oncology|February 1, 1989
The familial dysplastic nevus syndrome. Natural history and the impact of screening on prognosis. A study of nine families in the NetherlandsH F Vasen, W Bergman, A van Haeringen, et al.
American Journal of Medical Genetics|October 1, 1989
Intermittent thrombocytopenia and absent radii: report of a patient with additional unusual manifestationsA van Haeringen, F Veenstra, P D Maaswinkel-Mooij, et al.
Clinical Genetics|June 1, 1987
Autosomal dominant epidermolysis bullosa dystrophica: are the Cockayne-Touraine, the Pasini and the Bart-types different expressions of the same mutant gene?J N Bouwes Bavinck, A van Haeringen, D Ruiter, et al.
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
The Catel-Manzke syndrome in a female infantS G Kant, A Oudshoorn, C V Gi, et al.
Journal of Experimental Animal Science|January 1, 1996
Polymorphic microsatellite DNA markers in the rabbit (Oryctolagus cuniculus)W A van Haeringen, M den Bieman, L F van Zutphen, et al.
Human Genetics|September 1, 1988
Further evidence for localization of the gene of erythrokeratodermia variabilisJ G van der Schroeff, I van Leeuwen-Cornelisse, A van Haeringen, et al.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
Animal Genetics|November 1, 2011
Population studies of 17 equine STR for forensic and phylogenetic analysisL H P van de Goor, W A van Haeringen, J A Lenstra
Melanoma Research|June 4, 1998
Multiple agminate Spitz naeviM M Hulshof, A van Haeringen, N A Gruis, et al.
American Journal of Medical Genetics|December 2, 1996
Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotypeM C Lindeman-Kusse, A Van Haeringen, J J Hoorweg-Nijman, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 6, 1987
[Familial dysplastic nevus syndrome in the Netherlands; various clinical and genetic aspects]W Bergman, A Palan, A van Haeringen, et al.
European Journal of Cancer & Clinical Oncology|February 1, 1989
The familial dysplastic nevus syndrome. Natural history and the impact of screening on prognosis. A study of nine families in the NetherlandsH F Vasen, W Bergman, A van Haeringen, et al.
American Journal of Medical Genetics|October 1, 1989
Intermittent thrombocytopenia and absent radii: report of a patient with additional unusual manifestationsA van Haeringen, F Veenstra, P D Maaswinkel-Mooij, et al.
Clinical Genetics|June 1, 1987
Autosomal dominant epidermolysis bullosa dystrophica: are the Cockayne-Touraine, the Pasini and the Bart-types different expressions of the same mutant gene?J N Bouwes Bavinck, A van Haeringen, D Ruiter, et al.
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
The Catel-Manzke syndrome in a female infantS G Kant, A Oudshoorn, C V Gi, et al.
Journal of Experimental Animal Science|January 1, 1996
Polymorphic microsatellite DNA markers in the rabbit (Oryctolagus cuniculus)W A van Haeringen, M den Bieman, L F van Zutphen, et al.
Human Genetics|September 1, 1988
Further evidence for localization of the gene of erythrokeratodermia variabilisJ G van der Schroeff, I van Leeuwen-Cornelisse, A van Haeringen, et al.
Pageof 6