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W R Breg

Showing results (31-40 of 87) with videos related to

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Nature: New Biology|June 30, 1971
Distinctive fluorescence of quinacrine-labelled human G group chromosomesW R Breg, O J Miller, D A Miller, et al.
Nature|July 2, 1971
Quinacrine fluorescence patterns of human D group chromosomesD A Miller, P W Allderdice, O J Miller, et al.
Nature: New Biology|March 22, 1972
Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomesW R Breg, P W Alderdice, D A Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1976
Deletion of the short arm of chromosome 5 from a subject with cri-du-chat syndrome respository identification no. GM-71W R Breg, M M Aronson, A E Greene, et al.
American Journal of Medical Genetics|May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methodsL R Shapiro, P L Wilmot, P D Murphy, et al.
The Journal of Pediatrics|May 1, 1971
Partial deletion of short arm of chromosome no. 4J W Mace, M D Cunningham, O J Miller, et al.
American Journal of Medical Genetics|December 1, 1984
Cytogenetic diagnosis using midtrimester fetal blood samples: application to suspected mosaicism and other diagnostic problemsM S Watson, W R Breg, J C Hobbins, et al.
American Journal of Medical Genetics|April 1, 1991
"Pseudomosaicism" for 4p- in amniotic fluid cell culture proven to be true mosaicism after birthJ Vockley, J A Inserra, W R Breg, et al.
American Journal of Medical Genetics|June 15, 1991
Familial occurrence of esophageal atresia with and without tracheoesophagel fistula: report of two unusual kindredsB A Pletcher, J S Friedes, W R Breg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1974
Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13R O Howard, W R Breg, D M Albert, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
Nature: New Biology|June 30, 1971
Distinctive fluorescence of quinacrine-labelled human G group chromosomesW R Breg, O J Miller, D A Miller, et al.
Nature|July 2, 1971
Quinacrine fluorescence patterns of human D group chromosomesD A Miller, P W Allderdice, O J Miller, et al.
Nature: New Biology|March 22, 1972
Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomesW R Breg, P W Alderdice, D A Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1976
Deletion of the short arm of chromosome 5 from a subject with cri-du-chat syndrome respository identification no. GM-71W R Breg, M M Aronson, A E Greene, et al.
American Journal of Medical Genetics|May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methodsL R Shapiro, P L Wilmot, P D Murphy, et al.
The Journal of Pediatrics|May 1, 1971
Partial deletion of short arm of chromosome no. 4J W Mace, M D Cunningham, O J Miller, et al.
American Journal of Medical Genetics|December 1, 1984
Cytogenetic diagnosis using midtrimester fetal blood samples: application to suspected mosaicism and other diagnostic problemsM S Watson, W R Breg, J C Hobbins, et al.
American Journal of Medical Genetics|April 1, 1991
"Pseudomosaicism" for 4p- in amniotic fluid cell culture proven to be true mosaicism after birthJ Vockley, J A Inserra, W R Breg, et al.
American Journal of Medical Genetics|June 15, 1991
Familial occurrence of esophageal atresia with and without tracheoesophagel fistula: report of two unusual kindredsB A Pletcher, J S Friedes, W R Breg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1974
Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13R O Howard, W R Breg, D M Albert, et al.
Pageof 9