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HANNAH FIRTH, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1710747803Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Surveillance of working conditions and the work environment: development of a national hazard surveillance tool in New Zealand.
PMID 19636510·Int J Public Health·2010
8-other
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
PMID 19344873·Am J Hum Genet·2009
5-case
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.
PMID 19126570·J Med Genet·2009
8-other
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients.
PMID 19471318·Eur J Hum Genet·2009
5-case
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.
PMID 18622393·Nat Genet·2008
8-other
Syndromic associations with congenital anomalies of the fetal thorax and abdomen.
PMID 18634120·Prenat Diagn·2008
6-review
Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children.
PMID 17545556·J Med Genet·2007
5-case
Prenatal diagnosis of Harlequin ichthyosis presenting as distal arthrogryposis using three-dimensional ultrasound.
PMID 17385787·Prenat Diagn·2007
5-case
Cancer mortality by occupation among New Zealand women: 1988-1997.
PMID 18264202·N Z Med J·2007
8-other
Guidelines for molecular karyotyping in constitutional genetic diagnosis.
PMID 17637806·Eur J Hum Genet·2007
4-observational
Persistent upper airway obstruction is a diagnostic feature of spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type) with further evidence for dominant inheritance.
PMID 17676604·Am J Med Genet A·2007
5-case
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
PMID 16801345·J Med Genet·2007
8-other
ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.
PMID 16385466·Am J Hum Genet·2006
5-case
Dust and noise exposures among farmers in Southland,New Zealand.
PMID 16546808·Int J Environ Health Res·2006
4-observational
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.
PMID 16906163·Nat Genet·2006
4-observational
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome.
PMID 17041942·Am J Med Genet A·2006
5-case
Obtaining health information from farmers: interviews versus postal questionnaires in a New Zealand case study.
PMID 16457477·Ann Agric Environ Med·2005
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
- 725 NORTH STREET, DEPT. OF SURGERY WARRINER, 3RD FLOOR
PITTSFIELD, MA 01201 - Phone
- (413) 395-7916
Quick Facts
- NPI
- 1710747803
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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