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NATALIE NOWAK, MD
MD
Internal Medicine Physician
NPI: 1609767136Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
TRN43350(FL)
Research & Publications (20)
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.
PMID 19546099·J Med Genet·2010
5-case
Comparison of comparative genomic hybridization technologies across microarray platforms.
PMID 19503625·J Biomol Tech·2009
8-other
Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18.
PMID 19215787·Cancer Genet Cytogenet·2009
4-observational
Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations.
PMID 19672138·Psychiatr Genet·2009
8-other
Disruption of contactin 4 in three subjects with autism spectrum disorder.
PMID 18349135·J Med Genet·2009
8-other
Array-comparative genomic hybridization analysis of primary endometrial and ovarian high-grade neuroendocrine carcinoma associated with adenocarcinoma: mystery resolved?
PMID 18753966·Int J Gynecol Pathol·2008
8-other
Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay.
PMID 18627053·Am J Med Genet A·2008
4-observational
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
PMID 18374305·Biol Psychiatry·2008
8-other
Chromosome 11 genomic changes in parathyroid adenoma and hyperplasia: array CGH, FISH, and tissue microarrays.
PMID 18398822·Genes Chromosomes Cancer·2008
8-other
The use of array-based comparative genomic hybridization (a-CGH) to distinguish metastatic from primary synchronous carcinomas of the ovary and the uterus.
PMID 18643851·Histopathology·2008
8-other
A comparative analysis of two tissue procurement approaches for the genomic profiling of clinical colorectal cancer samples.
PMID 18629512·Int J Colorectal Dis·2008
4-observational
Intraperitoneal inflammation decreases endometriosis in a mouse model.
PMID 18653673·Hum Reprod·2008
7-preclinical
Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.
PMID 17412756·Hum Mol Genet·2007
7-preclinical
Comparative genomic instabilities of thyroid and colon cancers.
PMID 17515504·Arch Otolaryngol Head Neck Surg·2007
4-observational
Estimating the arm-wise false discovery rate in array comparative genomic hybridization experiments.
PMID 18052915·Stat Appl Genet Mol Biol·2007
8-other
Karyotypic changes detected by comparative genomic hybridization in a stillborn infant with chorioangioma and liver hemangioma.
PMID 17203486·Birth Defects Res A Clin Mol Teratol·2007
5-case
Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia.
PMID 17854671·Cancer Genet Cytogenet·2007
5-case
Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region.
PMID 17237124·J Med Genet·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 350 7TH ST N
NAPLES, FL 34102 - Phone
- (239) 624-0940
Quick Facts
- NPI
- 1609767136
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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