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American Journal of Medical Genetics
|
March 1, 1994
Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization
B R DuPont, R W Huff, L E Ridgway, et al.
Nucleic Acids Research
|
August 1, 1998
Cloning, chromosomal localization and promoter analysis of the human transcription factor YY1
Y L Yao, B R Dupont, S Ghosh, et al.
American Journal of Medical Genetics
|
July 17, 1995
Interstitial duplication 19p
R F Stratton, B R DuPont, A S Olsen, et al.
Genomics
|
August 1, 1996
Assignment of the human nuclear hormone receptor, NUC1 (PPARD), to chromosome 6p21.1-p21.2
T Yoshikawa, Z Brkanac, B R Dupont, et al.
Journal of Medical Genetics
|
December 10, 2002
Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype
V S Vervoort, D Viljoen, R Smart, et al.
Vox Sanguinis
|
January 1, 1995
Molecular characterization of glycophorin A transcripts in human erythroid cells using RT-PCR, allele-specific restriction, and sequencing
B R DuPont, S G Grant, S H Oto, et al.
American Journal of Medical Genetics
|
April 1, 1993
Trisomy 22 confirmed by fluorescent in situ hybridization
R F Stratton, B R DuPont, V L Mattern, et al.
Genomics
|
April 1, 1997
Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21
M MacDougall, B R DuPont, D Simmons, et al.
Radiation Research
|
October 1, 1993
Analysis of somatic cell mutations at the glycophorin A locus in atomic bomb survivors: a comparative study of assay methods
R G Langlois, M Akiyama, Y Kusunoki, et al.
Hematopathology and Molecular Hematology
|
January 1, 1997
Translocations of 11q13 in mantle cell lymphoma fail to disrupt the S mu bp-2 gene
M L Gulley, Q Zhang, R D Gascoyne, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
March 1, 1994
Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization
B R DuPont, R W Huff, L E Ridgway, et al.
Nucleic Acids Research
|
August 1, 1998
Cloning, chromosomal localization and promoter analysis of the human transcription factor YY1
Y L Yao, B R Dupont, S Ghosh, et al.
American Journal of Medical Genetics
|
July 17, 1995
Interstitial duplication 19p
R F Stratton, B R DuPont, A S Olsen, et al.
Genomics
|
August 1, 1996
Assignment of the human nuclear hormone receptor, NUC1 (PPARD), to chromosome 6p21.1-p21.2
T Yoshikawa, Z Brkanac, B R Dupont, et al.
Journal of Medical Genetics
|
December 10, 2002
Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype
V S Vervoort, D Viljoen, R Smart, et al.
Vox Sanguinis
|
January 1, 1995
Molecular characterization of glycophorin A transcripts in human erythroid cells using RT-PCR, allele-specific restriction, and sequencing
B R DuPont, S G Grant, S H Oto, et al.
American Journal of Medical Genetics
|
April 1, 1993
Trisomy 22 confirmed by fluorescent in situ hybridization
R F Stratton, B R DuPont, V L Mattern, et al.
Genomics
|
April 1, 1997
Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21
M MacDougall, B R DuPont, D Simmons, et al.
Radiation Research
|
October 1, 1993
Analysis of somatic cell mutations at the glycophorin A locus in atomic bomb survivors: a comparative study of assay methods
R G Langlois, M Akiyama, Y Kusunoki, et al.
Hematopathology and Molecular Hematology
|
January 1, 1997
Translocations of 11q13 in mantle cell lymphoma fail to disrupt the S mu bp-2 gene
M L Gulley, Q Zhang, R D Gascoyne, et al.
Page
of 3