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J Halley

Showing results (131-140 of 194) with videos related to

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The Journal of Biological Chemistry|August 15, 2002
Identification and characterization of the interaction between tuberin and 14-3-3zetaMark Nellist, Miriam A Goedbloed, Christa de Winter, et al.
Annals of Neurology|November 10, 2010
Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlationsMarlies J Valstar, Sanne Neijs, Hennie T Bruggenwirth, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.
American Journal of Medical Genetics. Part A|November 19, 2013
Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapseJan J J Aalberts, J Peter van Tintelen, Toon Oomen, 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.
Journal of Medical Genetics|October 1, 1995
General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutationB B de Vries, H Robinson, I Stolte-Dijkstra, 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.
American Journal of Medical Genetics|July 15, 1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, 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.
Pageof 20

Showing results (131-140 of 194) with videos related to

Sort By:
Pageof 20
The Journal of Biological Chemistry|August 15, 2002
Identification and characterization of the interaction between tuberin and 14-3-3zetaMark Nellist, Miriam A Goedbloed, Christa de Winter, et al.
Annals of Neurology|November 10, 2010
Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlationsMarlies J Valstar, Sanne Neijs, Hennie T Bruggenwirth, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.
American Journal of Medical Genetics. Part A|November 19, 2013
Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapseJan J J Aalberts, J Peter van Tintelen, Toon Oomen, 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.
Journal of Medical Genetics|October 1, 1995
General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutationB B de Vries, H Robinson, I Stolte-Dijkstra, 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.
American Journal of Medical Genetics|July 15, 1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, 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.
Pageof 20