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Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 12/2017, Volume 18, Issue 12, pp. 3457 - 3464
Objectives: Genetic markers are crucial fort diagnostic and prognostic investigation of hematological malignancies (HM). The conventional cytogenetic study... 
Chromosomal aberration | Cytogenetics | Hematological malignancies | Fluorescence in situ hybridization | fluorescence in situ hybridization | hematological malignancies | cytogenetics
Journal Article
Journal Article
Acta Medica International, ISSN 2349-0578, 07/2018, Volume 5, Issue 2, pp. 74 - 78
Aims: The aim of this study was to evaluate the complexity of the chromosomal abnormalities in multiple myeloma (MM) cases and to correlate the findings with... 
Complications and side effects | Genetic aspects | Chromosome abnormalities | Research | Risk factors | Multiple myeloma | Cytogenetics | Cell division | Chromosomes | Cloning | Age | Chromosomal aberrations in multiple myeloma | multiple myeloma | cytogenetic markers in multiple myeloma
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2008, Volume 26, Issue 15_suppl, pp. 18032 - 18032
Journal Article
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 2003, Volume 23, Issue 1-2, pp. 60 - 61
Journal Article
Fertility and Sterility, ISSN 0015-0282, 1988, Volume 49, Issue 5, pp. 917 - 919
We report on an Arab family in which a mother and two of her daughters, despite having deletion Xq25, are fertile. So far, only one case of deletion Xq25... 
Chromosome Deletion | Chromosome Banding | Fertility | Humans | Karyotyping | Middle Aged | X Chromosome | Adult | Female | Sex Chromosome Aberrations - genetics | Infertility, Female - genetics
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 02/1986, Volume 23, Issue 1, pp. 91 - 92
Journal Article
Journal Article
Cancer Genetics and Cytogenetics, ISSN 0165-4608, 1994, Volume 78, Issue 1, pp. 72 - 77
The expression of fragile sites (FS) in the blood lymphocytes of 54 individuals, including 11 retinoblastoma (Rb) patients, their clinically healthy family... 
Chromosome Deletion | Eye Neoplasms - genetics | Retinoblastoma - genetics | Humans | Chromosome Fragile Sites | Child, Preschool | Infant | Male | Chromosome Fragility | Karyotyping | Chromosomes, Human, Pair 13 | Female | Child
Journal Article
CANCER GENETICS AND CYTOGENETICS, ISSN 0165-4608, 11/1994, Volume 78, Issue 1, pp. 72 - 77
The expression of fragile sites (FS) in the blood lymphocytes of 54 individuals, including 11 retinoblastoma (Rb) patients, their clinically healthy family... 
BREAST-CANCER | ONCOLOGY | SUSCEPTIBILITY | GENETICS & HEREDITY | APHIDICOLIN | RENAL-CELL | CHROMOSOMES | REARRANGEMENTS | CARCINOMA | DELETION | BREAKPOINTS | LYMPHOCYTES
Journal Article
Cancer Genetics and Cytogenetics, ISSN 0165-4608, 04/2002, Volume 134, Issue 2, pp. 172 - 174
We report a case of acute myeloid leukemia (AML) [FAB-M5a] showing a deletion of the short arm of chromosome 2 at band p23 as a sole abnormality in the bone... 
ONCOLOGY | GENETICS & HEREDITY | Chromosome Deletion | Chromosomes, Human, Pair 2 - genetics | Chromosome Banding | Humans | Karyotyping | Male | Child | Leukemia, Myeloid, Acute - genetics
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 12/1987, Volume 24, Issue 12, pp. 784 - 786
A 13 year old female presented with ambiguous external genitalia, right inguinal ovotestis, left ovary, apparently normal Mullerian system, and absent Wolffian... 
Journal Article
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