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Cancer Genetics and Cytogenetics
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March 1, 1988
Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3
A H Puspurs, E Baker, D F Callen, et al.
Clinical Genetics
|
November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy
S Schuffenhauer, D F Callen, H Seidel, et al.
Genomics
|
September 1, 1994
Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2
I A Aksoy, D F Callen, S Apostolou, et al.
Genomics
|
August 1, 1991
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites
R I Richards, K Holman, S Lane, et al.
Journal of Human Genetics
|
November 26, 1999
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain
K Bhalla, H J Eyre, S A Whitmore, et al.
Genomics
|
June 6, 1998
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity
G Kremmidiotis, E Baker, J Crawford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24
M A Pritchard, E Baker, D F Callen, et al.
Clinical Genetics
|
June 1, 1994
Discordance between direct and PHA-stimulated chromosome preparations from neonates
I W Garnham, H Fernandez, D F Callen, et al.
Nucleic Acids Research
|
September 26, 1988
ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1
A Fratini, E G Baker, D F Callen, et al.
Nucleic Acids Research
|
September 26, 1988
RsaI and TaqI RFLPs for pACHF3.5 [D16S10]
A Fratini, E G Baker, D F Callen, et al.
Page
of 20
Search research articles
Search
Showing results (51-60 of 195) with videos related to
Sort By:
Page
of 20
Cancer Genetics and Cytogenetics
|
March 1, 1988
Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3
A H Puspurs, E Baker, D F Callen, et al.
Clinical Genetics
|
November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy
S Schuffenhauer, D F Callen, H Seidel, et al.
Genomics
|
September 1, 1994
Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2
I A Aksoy, D F Callen, S Apostolou, et al.
Genomics
|
August 1, 1991
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites
R I Richards, K Holman, S Lane, et al.
Journal of Human Genetics
|
November 26, 1999
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain
K Bhalla, H J Eyre, S A Whitmore, et al.
Genomics
|
June 6, 1998
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity
G Kremmidiotis, E Baker, J Crawford, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24
M A Pritchard, E Baker, D F Callen, et al.
Clinical Genetics
|
June 1, 1994
Discordance between direct and PHA-stimulated chromosome preparations from neonates
I W Garnham, H Fernandez, D F Callen, et al.
Nucleic Acids Research
|
September 26, 1988
ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1
A Fratini, E G Baker, D F Callen, et al.
Nucleic Acids Research
|
September 26, 1988
RsaI and TaqI RFLPs for pACHF3.5 [D16S10]
A Fratini, E G Baker, D F Callen, et al.
Page
of 20