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AURELIA MELONI-EHRIG, PH.D., D.SC.
PH.D., D.SC.
Clinical Cytogenetics Physician
NPI: 1942418603Individual
Specialties, Licenses & Credentials
Clinical Cytogenetics PhysicianPrimary
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
MELOA1(NY)
Research & Publications (17)
Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia.
PMID 19480935·Cancer Genet Cytogenet·2009
5-case
Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma.
PMID 19389508·Cancer Genet Cytogenet·2009
5-case
Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation.
PMID 19380032·Cancer Genet Cytogenet·2009
5-case
A case of lipoblastoma with seven copies of chromosome 8.
PMID 19264235·Cancer Genet Cytogenet·2009
5-case
Poor outcome in a pediatric patient with acute myeloid leukemia associated with a variant t(8;21) and trisomy 6.
PMID 19167612·Cancer Genet Cytogenet·2009
5-case
Synchronous development of acute myeloid leukemia in recipient and donor after allogeneic bone marrow transplantation: report of a case with comments on donor evaluation.
PMID 19040490·Transfusion·2009
5-case
Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.
PMID 17452260·Cancer Genet Cytogenet·2007
5-case
Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies.
PMID 16965957·Cancer Genet Cytogenet·2006
5-case
Benign chronic neutropenia with abnormalities involving 16q22, affecting mother and daughter.
PMID 16550514·Am J Hematol·2006
5-case
Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.
PMID 16080963·Cancer Genet Cytogenet·2005
5-case
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.
PMID 16080960·Cancer Genet Cytogenet·2005
5-case
Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogenetics.
PMID 11503167·Am J Med Genet·2001
5-case
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25.
PMID 11244503·Oncogene·2001
8-other
Malignant giant cell tumor of synovium (malignant pigmented villonodular synovitis).
PMID 11079016·Arch Pathol Lab Med·2000
5-case
Evidence by spectral karyotyping that 8q11.2 is nonrandomly involved in lipoblastoma.
PMID 11272891·J Mol Diagn·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2580 WESTSIDE PKWY
ALPHARETTA, GA 30004 - Phone
- (678) 319-3310
Quick Facts
- NPI
- 1942418603
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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