Qumsiyeh, Mazin B.
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Mazin Qumsiyeh Palestinian writer
Qumṣīyah, Māzin
Qumsiyeh, Mazin
VIAF ID: 18590680 (Personal)
Permalink: http://viaf.org/viaf/18590680
Preferred Forms
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Mazin Qumsiyeh
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Palestinian writer
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Qumsiyeh
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Mazin
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Qumsiyeh, Mazin B.
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100 1 _
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Qumsiyeh, Mazin B.
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100 1 _
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Qumsiyeh, Mazin B.
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100 1 _ ‡a Qumsiyeh, Mazin B.
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100 1 _ ‡a Qumsiyeh, Mazin B.
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100 1 _
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Qumṣīyah, Māzin
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100 1 _
‡a
Qumṣīyah, Māzin
4xx's: Alternate Name Forms (13)
Works
| Title | Sources |
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| Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders. |
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| Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi |
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| Assignment of human transforming growth factor-beta type I and type III receptor genes (TGFBR1 and TGFBR3) to 9q33-q34 and 1p32-p33, respectively |
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| Bat records from Mauritania, Africa (Mammalia: Chiroptera), 1981: |
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| The bats of Egypt |
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| Central review of cytogenetics is necessary for cooperative group correlative and clinical studies of adult acute leukemia: the Cancer and Leukemia Group B experience |
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| Clinical characteristics of patients with de novo acute myeloid leukaemia and isolated trisomy 11: a Cancer and Leukemia Group B study |
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| Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma. |
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| Cytogenetic abnormalities and the failure of development after round spermatid injections |
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| Cytogenetic data on the rodent family Gerbillidae |
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| Cytogenetics and mechanisms of spontaneous abortions: increased apoptosis and decreased cell proliferation in chromosomally abnormal villi. |
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| Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome |
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| Distal limb anomalies, Robin sequence, and deletions in 4q31-->qter |
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| Donor Y chromosome in renal carcinoma cells of a female BMT recipient: visualization of putative BMT-tumor hybrids by FISH |
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| Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy |
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| EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3 |
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| ETV6/CBFA2 fusions in childhood B-cell precursor acute lymphoblastic leukemia with myeloid markers |
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| Evidence for eight tandem and five centric fusions in the evolution of the karyotype of Aethomys namaquensis A. Smith (Rodentia: Muridae). |
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| Evolution of number and morphology of mammalian chromosomes. |
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| F-MuLV acceleration of myelomonocytic tumorigenesis in SV40 large T antigen transgenic mice is accompanied by retroviral insertion at Fli1 and a novel locus, Fim4. |
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| Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene |
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| Familial supernumerary marker chromosome evolution through three generations |
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| FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6. |
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| Gene amplification and chromosome rearrangements: a study of a single cell lineage selected for amplification and deamplification of the UMP synthase gene. |
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| Genome profiling of ovarian adenocarcinomas using pangenomic BACs microarray comparative genomic hybridization |
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| Genomic structure and chromosomal localization of the novel ETS factor, PE-2 (ERF). |
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| High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement. |
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| Une histoire populaire de la résistance palestinienne : l'espoir et l'autonomisation |
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| Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes |
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| Interphase detection of trisomy 12 in B-cell chronic lymphocytic leukemia by fluorescence hybridization in situ |
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| Kanaan: ein gemeinsames Land Menschenrechte und der israelisch-palästinenische Konflikt |
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| Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement. |
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| Localization of the adenosine deaminase, transferrin, and UMP synthetase genes on Chinese hamster chromosomes 4 and 6 by in situ hybridization. |
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| Mammals of the Holy Land |
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| Morphological and cytogenetic analysis of intact oocytes and blocked zygotes. |
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| al-Muqāwamah al-shaʻbīyah fī Filasṭīn, 2011: |
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| Natural killer cell lymphoma/leukemia with homozygous loss of p27/kip1. |
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| A novel chromosomal rearrangement associated with therapy-related acute leukemia |
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| A novel immortalized human endometrial stromal cell line with normal progestational response |
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| De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH. |
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| Numerical chromosome abnormalities associated with early clinical stages of gynecologic tumors |
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| Patients with t(8;21)(q22;q22) and acute myeloid leukemia have superior failure-free and overall survival when repetitive cycles of high-dose cytarabine are administered |
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| Popular resistance in Palestine : a history of hope and empowerment |
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| Postnatal developmental delay and chromosomal abnormalities. |
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| A potential model for early stages of chromosomal evolution via concentric Robertsonian fans: a large area of polymorphism in southern short-tailed shrews |
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| Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques |
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| Pretreatment cytogenetics add to other prognostic factors predicting complete remission and long-term outcome in patients 60 years of age or older with acute myeloid leukemia: results from Cancer and Leukemia Group B 8461. |
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| Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23). |
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| Real-time quantitative RT-PCR of cyclin D1 mRNA in mantle cell lymphoma: comparison with FISH and immunohistochemistry. |
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| RET/papillary thyroid cancer rearrangement in nonneoplastic thyrocytes: follicular cells of Hashimoto's thyroiditis share low-level recombination events with a subset of papillary carcinoma. |
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| Robertsonian chromosomal rearrangements in the short-tailed shrew, Blarina carolinensis, in western Tennessee |
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| Sensitivity and specificity of whole chromosome paint (WCP) probes are correlated with size of translocated segment. |
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| Sharing the land of Canaan : human rights and the Israeli-Palestinian struggle |
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| Structure and function of the nucleus: anatomy and physiology of chromatin. |
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| Syndromal frontonasal dysostosis in a child with a complex translocation involving chromosomes 3, 7, and 11. |
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| Telomerase prolongs the lifespan of normal human ovarian surface epithelial cells without inducing neoplastic phenotype. |
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| Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia with tetrasomy 8 |
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| Trisomy 6 acquired in lymphoid blast transformation of chronic myelocytic leukemia with t(9;22) |
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| Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. |
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| Unconjugated estriol as an indication for prenatal diagnosis of steroid sulfatase deficiency by in situ hybridization. |
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| Velo-facio-skeletal syndrome in a mother and daughter |
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| المقاومة الشعبية في فلسطين : تاريخ حافل بالامل والانجاز |
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