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C Modahl

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

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Psychological Review|July 1, 1996
Neurofunctional mechanisms in autismL Waterhouse, D Fein, C Modahl
Journal of Autism and Developmental Disorders|September 1, 1992
Does oxytocin deficiency mediate social deficits in autism?C Modahl, D Fein, L Waterhouse, et al.
Biological Psychiatry|November 3, 2001
Oxytocin and autistic disorder: alterations in peptide formsL Green, D Fein, C Modahl, et al.
Biological Psychiatry|March 26, 1998
Plasma oxytocin levels in autistic childrenC Modahl, L Green, D Fein, et al.
Cytogenetics and Cell Genetics|November 10, 2001
Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCRM Smith, J R Escamilla, P Filipek, et al.
American Journal of Medical Genetics|December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13M Smith, P A Filipek, C Wu, et al.
Cytogenetic and Genome Research|June 27, 2003
Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficitsM Smith, A Woodroffe, R Smith, et al.
Pageof 1

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

Sort By:
Pageof 1
Psychological Review|July 1, 1996
Neurofunctional mechanisms in autismL Waterhouse, D Fein, C Modahl
Journal of Autism and Developmental Disorders|September 1, 1992
Does oxytocin deficiency mediate social deficits in autism?C Modahl, D Fein, L Waterhouse, et al.
Biological Psychiatry|November 3, 2001
Oxytocin and autistic disorder: alterations in peptide formsL Green, D Fein, C Modahl, et al.
Biological Psychiatry|March 26, 1998
Plasma oxytocin levels in autistic childrenC Modahl, L Green, D Fein, et al.
Cytogenetics and Cell Genetics|November 10, 2001
Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCRM Smith, J R Escamilla, P Filipek, et al.
American Journal of Medical Genetics|December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13M Smith, P A Filipek, C Wu, et al.
Cytogenetic and Genome Research|June 27, 2003
Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficitsM Smith, A Woodroffe, R Smith, et al.
Pageof 1