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C O Carter

Showing results (61-70 of 79) with videos related to

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Monographs in Human Genetics|January 1, 1972
Immunoglobulin levels in dystrophia myotonicaS Bundey, C O Carter, J F Soothill
British Medical Journal (Clinical Research Ed.)|January 22, 1983
Effect of genetic counselling on the prevalence of Huntington's choreaC O Carter, K A Evans, M Baraitser
Journal of Medical Genetics|August 1, 1981
A family study of hydrocephalus resulting from aqueduct stenosisF M Howard, K Till, C O Carter
Lancet (London, England)|March 22, 1975
Letter: Neural-tube malformations in offspring of spina-bifida patientsC O Carter, K A Evans, S Campbell
Brain : a Journal of Neurology|September 1, 1973
The genetic identity of acute infantile spinal muscular atrophyJ H Pearn, C O Carter, J Wilson
Journal of Inherited Metabolic Disease|January 1, 1978
Birthweight of infants with phenylketonuria and their unaffected siblingsI Smith, C O Carter, O H Wolfe
Journal of Medical Genetics|June 1, 1978
Heterozygote advantage for the phenylketonuria alleleI Smith, C O Carter, O H Wolff
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1970
Early recognition of heterozygotes for the gene for dystrophia myotonicaS Bundey, C O Carter, J F Soothill
Journal of Medical Genetics|August 1, 1982
A family study of craniosynostosis, with probable recognition of a distinct syndromeC O Carter, K Till, V Fraser, et al.
British Medical Journal|September 4, 1976
Use of creatine kinase for detecting severe X-linked muscular dystrophy carriersN R Dennis, K Evans, B Clayton, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Monographs in Human Genetics|January 1, 1972
Immunoglobulin levels in dystrophia myotonicaS Bundey, C O Carter, J F Soothill
British Medical Journal (Clinical Research Ed.)|January 22, 1983
Effect of genetic counselling on the prevalence of Huntington's choreaC O Carter, K A Evans, M Baraitser
Journal of Medical Genetics|August 1, 1981
A family study of hydrocephalus resulting from aqueduct stenosisF M Howard, K Till, C O Carter
Lancet (London, England)|March 22, 1975
Letter: Neural-tube malformations in offspring of spina-bifida patientsC O Carter, K A Evans, S Campbell
Brain : a Journal of Neurology|September 1, 1973
The genetic identity of acute infantile spinal muscular atrophyJ H Pearn, C O Carter, J Wilson
Journal of Inherited Metabolic Disease|January 1, 1978
Birthweight of infants with phenylketonuria and their unaffected siblingsI Smith, C O Carter, O H Wolfe
Journal of Medical Genetics|June 1, 1978
Heterozygote advantage for the phenylketonuria alleleI Smith, C O Carter, O H Wolff
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1970
Early recognition of heterozygotes for the gene for dystrophia myotonicaS Bundey, C O Carter, J F Soothill
Journal of Medical Genetics|August 1, 1982
A family study of craniosynostosis, with probable recognition of a distinct syndromeC O Carter, K Till, V Fraser, et al.
British Medical Journal|September 4, 1976
Use of creatine kinase for detecting severe X-linked muscular dystrophy carriersN R Dennis, K Evans, B Clayton, et al.
Pageof 8