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CHANTELLE SHAW, DO
DO
NPI: 1447711585Individual
Specialties, Licenses & Credentials
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
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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