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DEREK WAGGONER, PHD
PHD
Clinical Laboratory Director (Non-physician)
NPI: 1336877042Individual
Specialties, Licenses & Credentials
Clinical Laboratory Director (Non-physician)Primary
Technician, Pathology — Clinical Laboratory Director, Non-physician
Code: 247ZC0005X
DI53685(FL)
Research & Publications (20)
Two Children with macrocephaly, developmental delay, and PTEN mutation.
PMID 18626099·Clin Pediatr (Phila)·2009
5-case
Mediastinal plasmacytoma detected by echocardiography and biopsied with EUS-FNA.
PMID 18771540·Echocardiography·2008
5-case
Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
PMID 18446860·Am J Med Genet A·2008
8-other
Implementing computerized physician order management at a community hospital.
PMID 18351192·Jt Comm J Qual Patient Saf·2008
8-other
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.
PMID 18203180·Am J Med Genet A·2008
5-case
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.
PMID 17431914·Am J Med Genet A·2007
5-case
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex.
PMID 17336067·Neuromuscul Disord·2007
8-other
Integration of internet-based genetic databases into the medical school pre-clinical and clinical curriculum.
PMID 16778600·Genet Med·2006
8-other
Hypernatremia after cleft lip repair in a patient with holoprosencephaly.
PMID 16492862·Anesth Analg·2006
5-case
Familial pyloric stenosis associated with developmental delays.
PMID 15990644·J Pediatr Gastroenterol Nutr·2005
5-case
NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.
PMID 16247291·Genet Med·2005
8-other
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome.
PMID 16183809·Pediatr Res·2005
4-observational
Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations.
PMID 15942875·Am J Hum Genet·2005
8-other
Calibration of 6q subtelomere deletions to define genotype/phenotype correlations.
PMID 15811006·Clin Genet·2005
5-case
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome.
PMID 15805156·J Med 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
- Address
- 1400 NW 12TH AVE STE 4065
MIAMI, FL 33136 - Phone
- (305) 243-6952
Quick Facts
- NPI
- 1336877042
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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