Dr. Andrew John pham Carroll MD
Family Practitioner
333 N Dobson Rd Suite 15 Chandler AZ, 85224About
Dr. Andrew Carroll is a family practitioner practicing in Chandler, AZ. Dr. Carroll specializes in comprehensive health care for people of all ages. In addition to diagnosing and treating illnesses, family practitioners also put focus on preventative care with routine checkups, tests and personalized coaching on how to maintain a healthy lifestyle. Dr. Carroll possesses immense general knowledge on maintaining health and today, family practitioners provide more care for the underserved and rural populations than any other medical specialty.
Education and Training
St George',s University
St George',s University 1996
St. George's University School of Medicine 1996
Board Certification
Family MedicineAmerican Board of Family MedicineABFM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
- Congenital diaphragmatic hernia: is 15q26.1-26.2 a candidate locus?
- Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).
- Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.
- Antimetabolite therapy for lesser-risk B-lineage acute lymphoblastic leukemia of childhood: a report from Children's Oncology Group Study P9201.
- Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
- A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.
- Distal 22q11.2 microduplication encompassing the BCR gene.
- Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia.
- Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication.
- Complex analysis of a recurrent pleomorphic hyalinizing angiectatic tumor of soft parts.
- Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
- The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.
- Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome.
- Family history of hematologic malignancies and risk of multiple myeloma: differences by race and clinical features.
Treatments
- Diabetes
- Sinusitis
- High Cholesterol
- Type 2 Diabetes
- Chronic Kidney Disease
- Hypothyroidism
- Pain
- Vascular Disease
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