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DANIELLE WAGGONER, MD
MD
Internal Medicine Physician
NPI: 1396935003Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
4301090543(MI)
Research & Publications (20)
Clinic-based study of plexiform neurofibromas in neurofibromatosis 1.
PMID 10797438·Am J Med Genet·2000
8-other
Brain copper content and cuproenzyme activity do not vary with prion protein expression level.
PMID 10713045·J Biol Chem·2000
7-preclinical
Two Children with macrocephaly, developmental delay, and PTEN mutation.
PMID 18626099·Clin Pediatr (Phila)·2009
5-case
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
Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
PMID 18446860·Am J Med Genet A·2008
8-other
Mediastinal plasmacytoma detected by echocardiography and biopsied with EUS-FNA.
PMID 18771540·Echocardiography·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
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
Familial pyloric stenosis associated with developmental delays.
PMID 15990644·J Pediatr Gastroenterol Nutr·2005
5-case
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 100 MICHIGAN ST NE, SUITE A721
GRAND RAPIDS, MI 49503 - Phone
- (616) 391-3139
Quick Facts
- NPI
- 1396935003
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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