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D Lindhout

Showing results (91-100 of 123) with videos related to

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Prenatal Diagnosis|May 1, 1990
Prenatal ultrasonographic diagnosis of radial-ray reduction malformationsJ T Brons, H J van der Harten, H P van Geijn, et al.
Genomics|October 1, 1990
Genetic heterogeneity in tuberous sclerosisL A Janssen, L A Sandkuyl, E C Merkens, et al.
Journal of Medical Genetics|August 6, 2002
Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndromeM M van Haelst, H J F M M Eussen, F Visscher, et al.
Journal of Medical Genetics|October 23, 1998
Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large familyS Verhoef, C T Schrander-Stumpel, V D Vuzevski, et al.
Lancet (London, England)|April 27, 1999
Peutz-Jeghers syndrome: 78-year follow-up of the original familyA M Westerman, M M Entius, E de Baar, et al.
Human Mutation|February 6, 1998
Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 geneS Verhoef, R Vrtel, L Bakker, et al.
American Journal of Medical Genetics|October 26, 1999
Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.
Human Mutation|July 17, 1999
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers familiesA M Westerman, M M Entius, P P Boor, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, E A Kvittingen, et al.
Genetic Testing|October 18, 2005
Large deletion at the TSC1 locus in a family with tuberous sclerosis complexM Nellist, O Sancak, M A Goedbloed, et al.
Pageof 13

Showing results (91-100 of 123) with videos related to

Sort By:
Pageof 13
Prenatal Diagnosis|May 1, 1990
Prenatal ultrasonographic diagnosis of radial-ray reduction malformationsJ T Brons, H J van der Harten, H P van Geijn, et al.
Genomics|October 1, 1990
Genetic heterogeneity in tuberous sclerosisL A Janssen, L A Sandkuyl, E C Merkens, et al.
Journal of Medical Genetics|August 6, 2002
Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndromeM M van Haelst, H J F M M Eussen, F Visscher, et al.
Journal of Medical Genetics|October 23, 1998
Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large familyS Verhoef, C T Schrander-Stumpel, V D Vuzevski, et al.
Lancet (London, England)|April 27, 1999
Peutz-Jeghers syndrome: 78-year follow-up of the original familyA M Westerman, M M Entius, E de Baar, et al.
Human Mutation|February 6, 1998
Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 geneS Verhoef, R Vrtel, L Bakker, et al.
American Journal of Medical Genetics|October 26, 1999
Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.
Human Mutation|July 17, 1999
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers familiesA M Westerman, M M Entius, P P Boor, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, E A Kvittingen, et al.
Genetic Testing|October 18, 2005
Large deletion at the TSC1 locus in a family with tuberous sclerosis complexM Nellist, O Sancak, M A Goedbloed, et al.
Pageof 13