284 results on '"Mikhail, Fady M"'
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2. The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors
3. DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism
4. Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
5. Outcomes of high-risk acute promyelocytic leukemia patients treated with arsenic trioxide (ATO)/all trans retinoic acid (ATRA) based induction and consolidation without maintenance phase: A case Series
6. Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia
7. Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndrome
8. Fragile Bones Secondary to SMURF1 Gene Duplication
9. Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group
10. DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism
11. Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome
12. Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC)
13. Inherited CSNK2A1 variants in families with Okur‐Chung neurodevelopmental syndrome
14. Enhanced targeting of CML stem and progenitor cells by inhibition of porcupine acyltransferase in combination with TKI
15. Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome.
16. Chromosomal Basis of Inheritance
17. List of Contributors
18. Family history of hematologic malignancies and risk of multiple myeloma : differences by race and clinical features
19. Utility of end of induction bone marrow biopsy and survival outcomes in acute promyelocytic leukemia treated with fixed-dose induction regimen.
20. Maternal uniparental isodisomy for chromosome 6 discovered by paternity testing: a case report
21. Diagnostic and Prognostic Utility of Fluorescence In situ Hybridization (FISH) Analysis in Acute Myeloid Leukemia
22. An in vivo model of glioblastoma radiation resistance identifies long noncoding RNAs and targetable kinases
23. Contributors
24. Chromosomes and Chromosomal Abnormalities
25. Transgenic Mice Overexpressing Neuregulin-1 Model Neurofibroma-Malignant Peripheral Nerve Sheath Tumor Progression and Implicate Specific Chromosomal Copy Number Variations in Tumorigenesis
26. Neuregulin-1 overexpression and Trp53 haploinsufficiency cooperatively promote de novo malignant peripheral nerve sheath tumor pathogenesis
27. Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia
28. Partial trisomy 21: A fifty-year follow-up visit
29. Sex-discordant monochorionic twins with blood and tissue chimerism
30. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
31. Palindrome-Mediated and Replication-Dependent Pathogenic Structural Rearrangements within the NF1 Gene
32. Therapy-related Myeloid Neoplasms in Children
33. Chromosomal Basis of Inheritance
34. Incidental Detection of Cancer Predisposition Gene Copy Number Variations by Array Comparative Genomic Hybridization
35. Chromosomes and Chromosomal Abnormalities
36. Contributors
37. The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cells
38. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
39. 9 - Chromosomal Basis of Inheritance
40. Central Nervous System Double Relapse of Acute Promyelocytic Leukemia and Acute Myelomonocytic Leukemia
41. Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication
42. Therapy-related Myeloid Neoplasms in Children: A Single-institute Study.
43. Distal 22q11.2 microduplication encompassing the BCR gene
44. Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities
45. A prenatally ascertained X;Y translocation characterized using conventional and molecular cytogenetics
46. Relapse after Prolonged Remission in Philadelphia-Like Acute Lymphoblastic Leukemia
47. A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene
48. Overlapping phenotype of Wolf–Hirschhorn and Beckwith–Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)
49. Complete Trisomy 17p Syndrome in a Girl With der(14)t(14;17)(p11.2;p11.2)
50. Menkes disease complicated by concurrent Koolen‐de Vries syndrome (17q21.31 deletion)
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