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WAQAAS AHMAD, MD
MD
Emergency Medicine Physician
NPI: 1538374707Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Detection of FLT3 oncogene mutations in acute myeloid leukemia using conformation sensitive gel electrophoresis.
PMID 19330068·Int J Mol Sci·2008
8-other
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.
PMID 18084694·J Hum Genet·2008
4-observational
Locating ethnicity and health: exploring concepts and contexts.
PMID 17986016·Sociol Health Illn·2007
6-review
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.
PMID 16932841·J Hum Genet·2006
8-other
A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly.
PMID 16900296·J Hum Genet·2006
5-case
Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
PMID 11337751·Am J Med Genet·2001
8-other
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
PMID 19229252·J Hum Genet·2009
8-other
A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin.
PMID 19674475·BMC Med Genet·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
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
- 3601 W 13 MILE RD
ROYAL OAK, MI 48073 - Phone
- (248) 551-0424
Quick Facts
- NPI
- 1538374707
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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