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T F Thurmon

Showing results (21-30 of 45) with videos related to

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American Journal of Human Genetics|September 1, 1979
Congenital universal muscular hypoplasia: evidence for autosomal recessive inheritanceM Z Pelias, T F Thurmon
Birth Defects Original Article Series|February 1, 1971
Two distinct types of autosomal dominant spastic paraplegiaT F Thurmon, B A Walker
Birth Defects Original Article Series|January 1, 1974
Genetic studies of the French-Acadians of LouisianaT F Thurmon, E B DeFraites
Public Health Reports (Washington, D.C. : 1974)|September 1, 1979
Genetic considerations in human cancer incidenceT F Thurmon, K P Robertson
The Journal of Clinical Pharmacology and New Drugs|October 1, 1972
Thioridazine and blast transformation. A negative reportG Arneson, C Marino, T F Thurmon
Birth Defects Original Article Series|January 1, 1976
Deafness and vitiligoT F Thurmon, J Jackson, C G Fowler
Birth Defects Original Article Series|January 1, 1975
Familial Prader-Willi syndromeE B DeFraites, T F Thurmon, H Farhadian
Birth Defects Original Article Series|January 1, 1974
Clinical heterogeneity in mucopolysaccharidosis. II. Evidence for epistasisT F Thurmon, E B DeFraites, E E Anderson
Birth Defects Original Article Series|January 1, 1975
Acrocephalosyndactyly and partial trisomy 6K P Robertson, T F Thurmon, M C Tracy
The Journal of Pediatrics|September 1, 1972
Phenobarbital and alkaline phosphatase: a preliminary reportT F Thurmon, K P Robertson, E E Anderson
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|September 1, 1979
Congenital universal muscular hypoplasia: evidence for autosomal recessive inheritanceM Z Pelias, T F Thurmon
Birth Defects Original Article Series|February 1, 1971
Two distinct types of autosomal dominant spastic paraplegiaT F Thurmon, B A Walker
Birth Defects Original Article Series|January 1, 1974
Genetic studies of the French-Acadians of LouisianaT F Thurmon, E B DeFraites
Public Health Reports (Washington, D.C. : 1974)|September 1, 1979
Genetic considerations in human cancer incidenceT F Thurmon, K P Robertson
The Journal of Clinical Pharmacology and New Drugs|October 1, 1972
Thioridazine and blast transformation. A negative reportG Arneson, C Marino, T F Thurmon
Birth Defects Original Article Series|January 1, 1976
Deafness and vitiligoT F Thurmon, J Jackson, C G Fowler
Birth Defects Original Article Series|January 1, 1975
Familial Prader-Willi syndromeE B DeFraites, T F Thurmon, H Farhadian
Birth Defects Original Article Series|January 1, 1974
Clinical heterogeneity in mucopolysaccharidosis. II. Evidence for epistasisT F Thurmon, E B DeFraites, E E Anderson
Birth Defects Original Article Series|January 1, 1975
Acrocephalosyndactyly and partial trisomy 6K P Robertson, T F Thurmon, M C Tracy
The Journal of Pediatrics|September 1, 1972
Phenobarbital and alkaline phosphatase: a preliminary reportT F Thurmon, K P Robertson, E E Anderson
Pageof 5