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N C Schanen

Showing results (1-10 of 14) with videos related to

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Journal of Child Neurology|December 30, 1999
Molecular approaches to the Rett syndrome geneN C Schanen
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Branchial cleft anomaly, congenital heart disease, and biliary atresia: Goldenhar complex or Lambert syndrome?J Cohen, N C Schanen
Brain Research. Molecular Brain Research|June 1, 1992
Isolation and characterization of microtubule-associated protein 2 (MAP2) kinase from rat brainN C Schanen, G Landreth
Molecular Genetics and Metabolism|March 6, 1999
Identification of a new polymorphism in the 3'-untranslated region of the human serotonin receptor 2C (5-HT2C) geneH R Song, A Gu, N C Schanen
Human Molecular Genetics|January 1, 1997
Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection methodS Hofferbert, N C Schanen, F Chehab, et al.
Neuropediatrics|June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?S Hofferbert, N C Schanen, S S Budden, et al.
Bone|May 6, 2009
Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndromeR D O'Connor, M Zayzafoon, M C Farach-Carson, et al.
British Journal of Haematology|July 10, 2001
Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndromeA A Thompson, K Woodruff, S A Feig, et al.
American Journal of Human Genetics|October 27, 1997
A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion mapN C Schanen, E J Dahle, F Capozzoli, et al.
Journal of Child Neurology|June 10, 1998
Neonatal encephalopathy in two boys in families with recurrent Rett syndromeN C Schanen, T W Kurczynski, D Brunelle, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Child Neurology|December 30, 1999
Molecular approaches to the Rett syndrome geneN C Schanen
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Branchial cleft anomaly, congenital heart disease, and biliary atresia: Goldenhar complex or Lambert syndrome?J Cohen, N C Schanen
Brain Research. Molecular Brain Research|June 1, 1992
Isolation and characterization of microtubule-associated protein 2 (MAP2) kinase from rat brainN C Schanen, G Landreth
Molecular Genetics and Metabolism|March 6, 1999
Identification of a new polymorphism in the 3'-untranslated region of the human serotonin receptor 2C (5-HT2C) geneH R Song, A Gu, N C Schanen
Human Molecular Genetics|January 1, 1997
Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection methodS Hofferbert, N C Schanen, F Chehab, et al.
Neuropediatrics|June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?S Hofferbert, N C Schanen, S S Budden, et al.
Bone|May 6, 2009
Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndromeR D O'Connor, M Zayzafoon, M C Farach-Carson, et al.
British Journal of Haematology|July 10, 2001
Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndromeA A Thompson, K Woodruff, S A Feig, et al.
American Journal of Human Genetics|October 27, 1997
A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion mapN C Schanen, E J Dahle, F Capozzoli, et al.
Journal of Child Neurology|June 10, 1998
Neonatal encephalopathy in two boys in families with recurrent Rett syndromeN C Schanen, T W Kurczynski, D Brunelle, et al.
Pageof 2