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Results: 1-16 |
Results: 16
Chromosome 7 heteromorphism
Authors: Mark, HFL
Citation: Hfl. Mark, Chromosome 7 heteromorphism, CANC GENET, 123(2), 2000, pp. 144-144
Constitutional mosaic trisomies, mutations, and deletions in cancer: A hypothesis
Authors: Mark, HFL
Citation: Hfl. Mark, Constitutional mosaic trisomies, mutations, and deletions in cancer: A hypothesis, CANC GENET, 121(1), 2000, pp. 103-105
Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting
Authors: Abuelo, DN Ahsanuddin, AN Mark, HFL
Citation: Dn. Abuelo et al., Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting, AM J MED G, 94(5), 2000, pp. 392-399
Fluorescence in situ hybridization (FISH) for detection of HER-2/neu amplification in breast cancer: A multicenter portability study
Authors: Persons, DL Bui, MM Lowery, MC Mark, HFL Yung, JF Birkmeier, JM Wong, EY Yang, SJ Masood, S
Citation: Dl. Persons et al., Fluorescence in situ hybridization (FISH) for detection of HER-2/neu amplification in breast cancer: A multicenter portability study, ANN CLIN L, 30(1), 2000, pp. 41-48
HER-2/neu gene amplification in stages I-IV breast cancer detected by fluorescent in situ hybridization
Authors: Mark, HFL Aswad, B Bassily, N Taylor, W Brown, S Sun, CL Samy, M Zolnierz, K Wong, E Bland, KI Hsu, PH
Citation: Hfl. Mark et al., HER-2/neu gene amplification in stages I-IV breast cancer detected by fluorescent in situ hybridization, GENET MED, 1(3), 1999, pp. 98-103
Conventional and molecular cytogenetic identification of a variant Klinefelter syndrome patient with a deleted X chromosome (vol 67, pg 55, 1999)
Authors: Mark, HFL
Citation: Hfl. Mark, Conventional and molecular cytogenetic identification of a variant Klinefelter syndrome patient with a deleted X chromosome (vol 67, pg 55, 1999), PATHOBIOLOG, 67(2), 1999, pp. 107-107
Trisomy 9 in a patient with secondary acute myelogenous leukemia detected by fluorescent in situ hybridization
Authors: Mark, HFL Gray, Y Sotomayor, E Joseph, P
Citation: Hfl. Mark et al., Trisomy 9 in a patient with secondary acute myelogenous leukemia detected by fluorescent in situ hybridization, PATHOBIOLOG, 67(2), 1999, pp. 111-114
Conventional and molecular cytogenetic identification of a variant Klinefelter syndrome patient with a deleted X chromosome
Authors: Mark, HFL Feldman, D Sigman, M
Citation: Hfl. Mark et al., Conventional and molecular cytogenetic identification of a variant Klinefelter syndrome patient with a deleted X chromosome, PATHOBIOLOG, 67(1), 1999, pp. 55-58
Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia
Authors: Sokolic, RA Ferguson, W Mark, HFL
Citation: Ra. Sokolic et al., Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia, CANC GENET, 115(2), 1999, pp. 106-113
Nonclonal aneuploidies and the tip of an iceberg revisited
Authors: Mark, HFL
Citation: Hfl. Mark, Nonclonal aneuploidies and the tip of an iceberg revisited, CANC GENET, 112(1), 1999, pp. 62-63
A multimodal approach in the diagnosis of patients with hematopoietic disorders
Authors: Mark, HFL Gray, Y Mark, Y Khorsand, J Sikov, W
Citation: Hfl. Mark et al., A multimodal approach in the diagnosis of patients with hematopoietic disorders, CANC GENET, 109(1), 1999, pp. 14-20
Trisomy 8 in embryonal rhabdomyosarcoma detected by fluorescence in situ hybridization
Authors: Afify, A Mark, HFL
Citation: A. Afify et Hfl. Mark, Trisomy 8 in embryonal rhabdomyosarcoma detected by fluorescence in situ hybridization, CANC GENET, 108(2), 1999, pp. 127-132
Trisomy 10 as a sole chromosomal abnormality in AML-M2
Authors: Estalilla, O Rintels, P Mark, HFL
Citation: O. Estalilla et al., Trisomy 10 as a sole chromosomal abnormality in AML-M2, CANC GENET, 108(2), 1999, pp. 175-175
Abnormal chromosome 8 copy number in stage I to stage IV breast cancer studied by fluorescence in situ hybridization
Authors: Mark, HFL Taylor, W Brown, S Samy, M Sun, CL Santoro, K Bland, KI
Citation: Hfl. Mark et al., Abnormal chromosome 8 copy number in stage I to stage IV breast cancer studied by fluorescence in situ hybridization, CANC GENET, 108(1), 1999, pp. 1-5
Study of chromosome 12 copy number in breast cancer using fluorescence in situ hybridization
Authors: Mark, HFL Brown, S Taylor, W Bassily, N Sun, CL Samy, M Bland, KI
Citation: Hfl. Mark et al., Study of chromosome 12 copy number in breast cancer using fluorescence in situ hybridization, CANC GENET, 108(1), 1999, pp. 26-31
Klinefelter syndrome
Authors: Mark, HFL Alter, D Mousseau, P
Citation: Hfl. Mark et al., Klinefelter syndrome, ARCH PATH L, 123(3), 1999, pp. 261-261
Risultati: 1-16 |