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SANDRA CHERN, M.D.
M.D.
Ophthalmology Physician
NPI: 1417957515Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
MD60576024(WA)
Research & Publications (20)
Methicillin-resistant Staphylococcus aureus retropharyngeal abscess complicated by a cervical spinal subdural empyema.
PMID 19013810·J Clin Neurosci·2009
5-case
Molecular prenatal diagnosis of thalassemia in Taiwan.
PMID 10802076·Int J Gynaecol Obstet·2000
8-other
Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites.
PMID 19346201·Taiwan J Obstet Gynecol·2009
5-case
Conformity of LINAC-based stereotactic radiosurgery using dynamic conformal arcs and micro-multileaf collimator.
PMID 18565688·Int J Radiat Oncol Biol Phys·2009
8-other
Structural organization of WrbA in apo- and holoprotein crystals.
PMID 19665595·Biochim Biophys Acta·2009
8-other
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
PMID 18661486·Prenat Diagn·2008
5-case
NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
PMID 18383001·Prenat Diagn·2008
5-case
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.
PMID 18400591·Taiwan J Obstet Gynecol·2008
5-case
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings.
PMID 18619002·Genet Couns·2008
5-case
Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13.
PMID 18400592·Taiwan J Obstet Gynecol·2008
5-case
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
PMID 18395879·Prenat Diagn·2008
5-case
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
PMID 18304539·Fertil Steril·2008
5-case
Sensitive and broadly reactive reverse transcription-PCR assays to detect novel paramyxoviruses.
PMID 18579717·J Clin Microbiol·2008
8-other
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
PMID 17953951·Fertil Steril·2008
5-case
Novalis intensity-modulated radiosurgery: methods for pretreatment planning.
PMID 18580777·Neurosurgery·2008
8-other
High proportion of single CYP2D6 gene deletion in Chinese attention-deficit-hyperactivity disorder children and its risk in oppositional defiant disorder.
PMID 19068017·Psychiatry Clin Neurosci·2008
8-other
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer.
PMID 18004080·Oncology·2007
8-other
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.
PMID 17962112·Taiwan J Obstet Gynecol·2007
5-case
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.
PMID 17962111·Taiwan J Obstet Gynecol·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 317 N DELAWARE ST
KENNEWICK, WA 99336 - Phone
- (509) 736-5550
Quick Facts
- NPI
- 1417957515
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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