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ALAN DONNENFELD, M.D.
M.D.
NPI: 1205894219IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
MT006828T(PA)25MA04955700(NJ)205012-1(NY)C1-0006729(DE)153714(MA)037414(CT)MD027052E(PA)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
GEISEL SCHOOL OF MEDICINE AT DARTMOUTH
Class of 1981
Research & Publications (20)
Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency.
PMID 16458654·Am J Obstet Gynecol·2006
8-other
Cytogenetics and molecular cytogenetics in prenatal diagnosis.
PMID 12848454·Clin Lab Med·2003
6-review
Biochemical screening for aneuploidy in ovum donor pregnancies.
PMID 12439508·Am J Obstet Gynecol·2002
8-other
Prenatal diagnosis from cystic hygroma fluid: the value of fluorescence in situ hybridization.
PMID 11641692·Am J Obstet Gynecol·2001
8-other
Comparison of modes of ascertainment for mosaic vs complete trisomy 21.
PMID 19318154·Am J Obstet Gynecol·2009
4-observational
Advanced maternal age as a sole indication for genetic amniocentesis; risk-benefit analysis based on a large database reflecting the current common practice.
PMID 18999912·J Perinat Med·2009
8-other
Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
PMID 18310361·Obstet Gynecol·2008
8-other
Quality assessment of routine nuchal translucency measurements: a North American laboratory perspective.
PMID 18281921·Genet Med·2008
4-observational
The risk of a major trisomy in fetuses with pyelectasis: the impact of an abnormal maternal serum screen or additional sonographic markers.
PMID 17466669·Am J Obstet Gynecol·2007
8-other
Characteristics and perspectives of families waiting to adopt a child with Down syndrome.
PMID 17438388·Genet Med·2007
8-other
Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion.
PMID 17099929·Prenat Diagn·2006
5-case
Global experience with Xibrom (bromfenac ophthalmic solution) 0.09%: the first twice-daily ophthalmic nonsteroidal anti-inflammatory drug.
PMID 17060789·Int Ophthalmol Clin·2006
6-review
Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
PMID 16582126·Obstet Gynecol·2006
4-observational
Sequential Down syndrome screening: the importance of first and second trimester test correlations when calculating risk.
PMID 16388325·J Genet Couns·2005
8-other
Fragile X syndrome carrier screening in the prenatal genetic counseling setting.
PMID 15834242·Genet Med·2005
8-other
Prenatal screening for Down syndrome should focus on safety more than cost-effectiveness.
PMID 15672045·Am J Obstet Gynecol·2005
8-other
Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies.
PMID 14708100·Am J Med Genet A·2004
5-case
Lipopolysaccharide-binding protein in microbial invasion of the amniotic cavity and human parturition.
PMID 12607763·J Matern Fetal Neonatal Med·2002
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
- 450 CRESSON BLVD STE 300
PHOENIXVILLE, PA 19460 - Phone
- (484) 831-0200
Quick Facts
- NPI
- 1205894219
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 7
- Locations
- 1
- Years in Practice
- 45
- Publications
- 20
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