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HANNAH STARKE, MD
MD
Pediatric Emergency Medicine (Pediatrics) Physician
NPI: 1588126585Individual
Specialties, Licenses & Credentials
Pediatric Emergency Medicine (Pediatrics) PhysicianPrimary
Pediatrics — Pediatric Emergency Medicine
Code: 2080P0204X
66061(AZ)V5837(TX)
Pediatrics Physician
Pediatrics
Code: 208000000X
66061(AZ)
Research & Publications (20)
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
PMID 19480690·Mol Cytogenet·2009
8-other
Array painting using microdissected chromosomes to map chromosomal breakpoints.
PMID 17317954·Cytogenet Genome Res·2007
8-other
Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
PMID 17451694·Fertil Steril·2007
5-case
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
PMID 17546703·Prenat Diagn·2007
5-case
Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males.
PMID 18160778·Cytogenet Genome Res·2007
8-other
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
PMID 16333826·Am J Med Genet A·2006
5-case
Analysis of non-crossover bivalents in pachytene cells from 10 normal men.
PMID 16751649·Hum Reprod·2006
8-other
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
PMID 16954677·Cytogenet Genome Res·2006
5-case
Variation in MLH1 distribution in recombination maps for individual chromosomes from human males.
PMID 16803849·Hum Mol Genet·2006
4-observational
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.
PMID 16954660·Cytogenet Genome Res·2006
6-review
Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
PMID 16954674·Cytogenet Genome Res·2006
5-case
Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect.
PMID 16954678·Cytogenet Genome Res·2006
5-case
A molecular cytogenetic study of chromosome evolution in chimpanzee.
PMID 16276092·Cytogenet Genome Res·2006
7-preclinical
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
PMID 16276087·Cytogenet Genome Res·2006
8-other
Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.
PMID 16954673·Cytogenet Genome Res·2006
8-other
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
PMID 16103662·Cytogenet Genome Res·2005
5-case
Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.
PMID 16126755·Hum Reprod·2005
8-other
Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males.
PMID 16155114·Hum Mol Genet·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 4 locations total
- Address
- 1 BAYLOR PLZ
HOUSTON, TX 77030 - Phone
- (713) 798-4951
Quick Facts
- NPI
- 1588126585
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 4
- Publications
- 20
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