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P W Allderdice

Showing results (21-30 of 38) with videos related to

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Nucleic Acids Research|September 25, 1991
The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPsP J McAlpine, M Dixon, P W Allderdice, et al.
American Journal of Human Genetics|September 1, 1979
Assignment of the red cell antigen, Targett (Rh40), to the Rh blood group systemM Lewis, H Kaita, P W Allderdice, et al.
Science (New York, N.Y.)|July 16, 1971
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cellsO J Miller, P W Allderdice, D A Miller, et al.
American Journal of Human Genetics|September 1, 1983
Duplication 9q34 syndromeP W Allderdice, B Eales, H Onyett, et al.
Cytogenetics|January 1, 1971
Quinacrine fluorescent karyotypes of human diploid and heteroploid cell linesO J Miller, D A Miller, P W Allderdice, et al.
The Journal of Pediatrics|November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)W R Breg, M W Steele, O J Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
Humangenetik|January 1, 1971
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescenceP W Allderdice, O J Miller, D A Miller, et al.
Genomics|October 1, 1991
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26P W Allderdice, H A Gardner, D Galutira, et al.
Archives of Dermatology|December 1, 1985
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pterJ B Ross, P W Allderdice, L J Shapiro, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Nucleic Acids Research|September 25, 1991
The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPsP J McAlpine, M Dixon, P W Allderdice, et al.
American Journal of Human Genetics|September 1, 1979
Assignment of the red cell antigen, Targett (Rh40), to the Rh blood group systemM Lewis, H Kaita, P W Allderdice, et al.
Science (New York, N.Y.)|July 16, 1971
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cellsO J Miller, P W Allderdice, D A Miller, et al.
American Journal of Human Genetics|September 1, 1983
Duplication 9q34 syndromeP W Allderdice, B Eales, H Onyett, et al.
Cytogenetics|January 1, 1971
Quinacrine fluorescent karyotypes of human diploid and heteroploid cell linesO J Miller, D A Miller, P W Allderdice, et al.
The Journal of Pediatrics|November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)W R Breg, M W Steele, O J Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
Humangenetik|January 1, 1971
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescenceP W Allderdice, O J Miller, D A Miller, et al.
Genomics|October 1, 1991
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26P W Allderdice, H A Gardner, D Galutira, et al.
Archives of Dermatology|December 1, 1985
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pterJ B Ross, P W Allderdice, L J Shapiro, et al.
Pageof 4