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A Palan

Showing results (1-10 of 7) with videos related to

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Human Genetics|October 1, 1987
Premature centromere division (PCD): a dominantly inherited cytogenetic anomalyK Madan, D Lindhout, A Palan
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1989
Studies on Leber's optic neuropathy IIIA Palan, A Stehouwer, L N Went
Annals of Human Genetics|July 1, 1986
Clinical and genetic studies in six Dutch kindreds with the dysplastic naevus syndromeW Bergman, A Palan, L N Went
Human Genetics|June 1, 1991
Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(I) chainA C Nicholls, J Oliver, D V Renouf, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
Journal of Palliative Medicine|February 2, 2018
Perspectives on Palliative Care in Cancer Clinical Trials: Diverse Meanings from Multidisciplinary Cancer Care ProvidersMichelle A Mollica, Erin E Kent, Kathleen M Castro, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Human Genetics|October 1, 1987
Premature centromere division (PCD): a dominantly inherited cytogenetic anomalyK Madan, D Lindhout, A Palan
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1989
Studies on Leber's optic neuropathy IIIA Palan, A Stehouwer, L N Went
Annals of Human Genetics|July 1, 1986
Clinical and genetic studies in six Dutch kindreds with the dysplastic naevus syndromeW Bergman, A Palan, L N Went
Human Genetics|June 1, 1991
Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(I) chainA C Nicholls, J Oliver, D V Renouf, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
Journal of Palliative Medicine|February 2, 2018
Perspectives on Palliative Care in Cancer Clinical Trials: Diverse Meanings from Multidisciplinary Cancer Care ProvidersMichelle A Mollica, Erin E Kent, Kathleen M Castro, et al.
Pageof 1