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SHEILA DOBIN, PHD
PHD
Ph.D. Medical Genetics Physician
NPI: 1922078187Individual
Specialties, Licenses & Credentials
Clinical Cytogenetics Physician
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
870096(MD)
Ph.D. Medical Genetics PhysicianPrimary
Medical Genetics — Ph.D. Medical Genetics
Code: 207SG0205X
1648(MD)
Research & Publications (17)
Translocation (10;14)(q24;q32) as the sole chromosomal abnormality in a metastatic follicular thyroid carcinoma.
PMID 19264233·Cancer Genet Cytogenet·2009
5-case
Leiomyoma of the urinary bladder: a cytogenetic study of a case.
PMID 17854672·Cancer Genet Cytogenet·2007
5-case
A clonal t(8;12)(p11.2;q24.3) as the sole abnormality in a solitary fibrous tumor of the pleura.
PMID 17175385·Cancer Genet Cytogenet·2007
5-case
Deletion (21)(q21.2q22.12) as a sole clonal cytogenetic abnormality in a lobular capillary hemangioma of the nasal cavity.
PMID 16965959·Cancer Genet Cytogenet·2006
5-case
A clonal translocation (7;8)(p13;q11.2) in a leiomyoma of the vulva.
PMID 16965956·Cancer Genet Cytogenet·2006
5-case
Cyclophosphamide followed by fludarabine for untreated chronic lymphocytic leukemia: a phase II SWOG TRIAL 9706.
PMID 16193091·Leukemia·2005
3-trial
A clonal dic(16;21)(p13.1;p11.2)del(16)(q11.1), with gains of several chromosomes and monosomy 21, in a case of splenic hamartoma: evidence for its neoplastic, not hamartomatous, origin.
PMID 15721639·Cancer Genet Cytogenet·2005
5-case
Primary myeloid sarcoma of the testicle with t(15;17).
PMID 15721636·Cancer Genet Cytogenet·2005
5-case
Overexpression of the BCL2 gene in a Sertoli-Leydig cell tumor of the ovary: a pathologic and cytogenetic study.
PMID 14734221·Cancer Genet Cytogenet·2004
8-other
Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma.
PMID 12868036·Ophthalmic Genet·2003
5-case
Clonal rearrangement of 15p11.2, 16p11.2, and 16p13.3 in a case of nodular fasciitis: additional evidence favoring nodular fasciitis as a benign neoplasm and not a reactive tumefaction.
PMID 12550774·Cancer Genet Cytogenet·2002
5-case
Isochromosome (17)(q10) as the sole structural chromosomal rearrangement in a case of botryoid rhabdomyosarcoma.
PMID 11454423·Cancer Genet Cytogenet·2001
5-case
Translocation (2;15)(p23;q21.2) and interstitial deletion of 7q in a case of low-grade myxofibrosarcoma.
PMID 11425453·Cancer Genet Cytogenet·2001
5-case
Trisomy 15 is frequently observed as a minor clone in patients with Anemia/MDS/NHL and as a major clone in patients with AML.
PMID 11063805·Cancer Genet Cytogenet·2000
8-other
Sclerosing epithelioid fibrosarcoma: a cytogenetic, immunohistochemical, and ultrastructural study of an unusual histological variant.
PMID 10867148·Cancer Genet Cytogenet·2000
5-case
Translocation (8;13)(q24.2;q33) in a malignant rhabdoid tumor of the liver.
PMID 10640148·Cancer Genet Cytogenet·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
- SCOTT AND WHITE CLINIC, 2401 S 31ST STREET
TEMPLE, TX 76508 - Phone
- (254) 724-3704
Quick Facts
- NPI
- 1922078187
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 17
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