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M G Butler

Showing results (1-10 of 212) with videos related to

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American Journal of Medical Genetics|May 8, 1995
High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndromeM G Butler
American Journal of Medical Genetics|January 11, 1996
Molecular diagnosis of Prader-Willi syndrome: comparison of cytogenetic and molecular genetic data including parent of origin dependent methylation DNA patternsM G Butler
American Journal of Human Genetics|July 1, 1989
Hypopigmentation: a common feature of Prader-Labhart-Willi syndromeM G Butler
Medical Laboratory Technology|April 1, 1973
A new method of hydrolysis for the identification of acid glycoproteinM G Butler
Comprehensive Therapy|July 1, 1988
Fragile X syndrome: a major cause of X-linked mental retardationM G Butler
American Journal of Medical Genetics|March 1, 1990
Prader-Willi syndrome: current understanding of cause and diagnosisM G Butler
American Journal of Medical Genetics|October 15, 1994
Trisomy 18 mosaicism in a 24-year-old white woman with normal intelligence and skeletal abnormalitiesM G Butler
The Nebraska Medical Journal|February 1, 1981
Sister chromatid exchange analysis in a 61 year-old female using various medicationsM G Butler
Mutation Research|July 1, 1981
Sister-chromatid exchange in 4 human racesM G Butler
Human Genetics|January 1, 1990
No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndromeM G Butler
Pageof 22

Showing results (1-10 of 212) with videos related to

Sort By:
Pageof 22
American Journal of Medical Genetics|May 8, 1995
High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndromeM G Butler
American Journal of Medical Genetics|January 11, 1996
Molecular diagnosis of Prader-Willi syndrome: comparison of cytogenetic and molecular genetic data including parent of origin dependent methylation DNA patternsM G Butler
American Journal of Human Genetics|July 1, 1989
Hypopigmentation: a common feature of Prader-Labhart-Willi syndromeM G Butler
Medical Laboratory Technology|April 1, 1973
A new method of hydrolysis for the identification of acid glycoproteinM G Butler
Comprehensive Therapy|July 1, 1988
Fragile X syndrome: a major cause of X-linked mental retardationM G Butler
American Journal of Medical Genetics|March 1, 1990
Prader-Willi syndrome: current understanding of cause and diagnosisM G Butler
American Journal of Medical Genetics|October 15, 1994
Trisomy 18 mosaicism in a 24-year-old white woman with normal intelligence and skeletal abnormalitiesM G Butler
The Nebraska Medical Journal|February 1, 1981
Sister chromatid exchange analysis in a 61 year-old female using various medicationsM G Butler
Mutation Research|July 1, 1981
Sister-chromatid exchange in 4 human racesM G Butler
Human Genetics|January 1, 1990
No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndromeM G Butler
Pageof 22