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CHANTELLE SHAW, DO
DO
NPI: 1447711585Individual
Specialties, Licenses & Credentials
Child & Adolescent Psychiatry PhysicianPrimary
Psychiatry & Neurology — Child & Adolescent Psychiatry
Code: 2084P0804X
T8942(TX)
Research & Publications (20)
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms.
PMID 15526218·Hum Genet·2005
8-other
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.
PMID 14764619·Hum Mol Genet·2004
6-review
A girl with duplication 17p10-p12 associated with a dicentric chromosome.
PMID 14699617·Am J Med Genet A·2004
5-case
Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders.
PMID 14757858·J Med Genet·2004
4-observational
Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substrates.
PMID 15148657·Am J Hum Genet·2004
4-observational
Small marker chromosomes in two patients with segmental aneusomy for proximal 17p.
PMID 15098121·Hum Genet·2004
5-case
Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.
PMID 12375235·Am J Hum Genet·2002
8-other
Symptomatic intra-cardiac metastasis complicating non-small cell lung cancer: imaging findings and clinical course.
PMID 18956220·Ir J Med Sci·2011
5-case
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.
PMID 19525032·Neurobiol Aging·2011
8-other
Concealed antegrade penetration of the atrio-ventricular node.
PMID 19608289·Int J Cardiol·2011
5-case
Assay reproducibility and within-person variation of Müllerian inhibiting substance.
PMID 19409547·Fertil Steril·2010
4-observational
Overexpression of the lily p70(s6k) gene in Arabidopsis affects elongation of flower organs and indicates TOR-dependent regulation of AP3, PI and SUP translation.
PMID 19651701·Plant Cell Physiol·2009
8-other
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
PMID 19451621·Proc Natl Acad Sci U S A·2009
8-other
Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes.
PMID 19546809·Genet Med·2009
8-other
(Mis)classification of ethnicity on the New Zealand Cancer Registry: 1981-2004.
PMID 19465958·N Z Med J·2009
4-observational
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.
PMID 19459885·Clin Genet·2009
5-case
TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
PMID 19496940·Neuropathology·2009
8-other
The primary locus of motor neuron death in an ALS-PDC mouse model.
PMID 19633581·Neuroreport·2009
7-preclinical
Compound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis.
PMID 19625994·Kidney Int·2009
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3120 SOUTHWEST FWY, STE 101 PMB 173354
HOUSTON, TX 77098 - Phone
- (832) 793-7942
Quick Facts
- NPI
- 1447711585
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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