Found: 23
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Relationship of LRP5rs121908669(G171R) genotypes to femur T-score values.
- Published in:
- Journal of Pharmaceutical Negative Results, 2023, v. 14, n. 3, p. 1224, doi. 10.47750/pnr.2023.14.03.163
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- Publication type:
- Article
De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case.
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- Journal of Reproduction & Infertility, 2018, v. 19, n. 1, p. 61
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- Article
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 2, p. 1, doi. 10.1002/mgg3.1854
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- Publication type:
- Article
Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report.
- Published in:
- 2016
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- Publication type:
- journal article
Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report.
- Published in:
- 2017
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- Publication type:
- journal article
A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13039-020-00512-3
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- Publication type:
- Article
An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case.
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- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00499-x
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- Publication type:
- Article
Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women.
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- Reproductive Sciences, 2017, v. 24, n. 9, p. 1275, doi. 10.1177/1933719116682874
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- Article
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44).
- Published in:
- 2018
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- Publication type:
- Case Study
Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment.
- Published in:
- Molecular Cytogenetics (17558166), 2015, v. 8, p. 1, doi. 10.1186/s13039-015-0204-x
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- Publication type:
- Article
Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event.
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- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0165-0
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- Publication type:
- Article
Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phasechronic myeloid leukemia case.
- Published in:
- 2014
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- Publication type:
- Case Study
An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations.
- Published in:
- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0060-0
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- Publication type:
- Article
Acquired del(9)(p22.3) in a primary plasma cell leukemia.
- Published in:
- 2013
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- Publication type:
- Case Study
A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints.
- Published in:
- Molecular Cytogenetics (17558166), 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8166-6-18
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- Publication type:
- Article
A novel dic (17;18) (p13.1;q11.2) with loss of TP53 and BCR/ABL rearrangement in an Imatinib resistant chronic myeloid leukemia.
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- Molecular Cytogenetics (17558166), 2012, v. 5, n. 1, p. 36, doi. 10.1186/1755-8166-5-36
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- Publication type:
- Article
Investigation of some genetic variations in BMP15 accompanied with premature ovarian failure (POF) in Syrian women.
- Published in:
- Middle East Fertility Society Journal, 2015, v. 20, n. 2, p. 91, doi. 10.1016/j.mefs.2014.02.005
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- Publication type:
- Article
A new case of de novo translocation (12;17;18)(q21.2;q22;q21.1) and cranio-cerebello-cardiac (3C) syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 3, p. 648, doi. 10.1002/ajmg.a.33742
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- Publication type:
- Article
De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report.
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- Oncology Letters, 2014, v. 7, n. 3, p. 787, doi. 10.3892/ol.2014.1784
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- Publication type:
- Article
De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report.
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- Journal of Medical Case Reports, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s13256-020-02587-3
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- Publication type:
- Article
De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report.
- Published in:
- 2021
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- Publication type:
- journal article
Influence of CYP1A1, GST polymorphisms and susceptibility risk of chronic myeloid leukemia in Syrian population.
- Published in:
- Medical Oncology, 2014, v. 31, n. 5, p. 1, doi. 10.1007/s12032-014-0889-4
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- Publication type:
- Article
Chromosomal aberration leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring; Report of a Syrian couple and review of the literature.
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- National Journal of Andrology / Zhonghua Nankexue, 2015, v. 21, n. 3, p. 219, doi. 10.13263/j.cnki.nja.2015.03.005
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- Publication type:
- Article