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Showing results (21-30 of 26) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1984
Ophthalmic manifestations of infantile phytanic acid storage diseaseR G Weleber, A C Tongue, N G Kennaway, et al.
Developmental Medicine and Child Neurology|April 1, 1986
Effects of fenfluramine on eight outpatients with the syndrome of autismE G Stubbs, S S Budden, R H Jackson, et al.
Autism Research and Treatment|April 17, 2015
Early Intervention with a Parent-Delivered Massage Protocol Directed at Tactile Abnormalities Decreases Severity of Autism and Improves Child-to-Parent Interactions: A Replication StudyLouisa M T Silva, Mark Schalock, Kristen R Gabrielsen, et al.
American Journal of Medical Genetics|March 1, 1990
Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequencesR E Magenis, S Toth-Fejel, L J Allen, et al.
American Journal of Human Genetics|December 1, 1999
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspotsM Wan, S S Lee, X Zhang, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1984
Ophthalmic manifestations of infantile phytanic acid storage diseaseR G Weleber, A C Tongue, N G Kennaway, et al.
Developmental Medicine and Child Neurology|April 1, 1986
Effects of fenfluramine on eight outpatients with the syndrome of autismE G Stubbs, S S Budden, R H Jackson, et al.
Autism Research and Treatment|April 17, 2015
Early Intervention with a Parent-Delivered Massage Protocol Directed at Tactile Abnormalities Decreases Severity of Autism and Improves Child-to-Parent Interactions: A Replication StudyLouisa M T Silva, Mark Schalock, Kristen R Gabrielsen, et al.
American Journal of Medical Genetics|March 1, 1990
Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequencesR E Magenis, S Toth-Fejel, L J Allen, et al.
American Journal of Human Genetics|December 1, 1999
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspotsM Wan, S S Lee, X Zhang, et al.
Brain & Development|May 30, 2001
Guidelines for reporting clinical features in cases with MECP2 mutationsA M Kerr, Y Nomura, D Armstrong, et al.
Pageof 3