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GHAZANFAR ALI, M.D.
M.D.
Family Medicine Physician
NPI: 1063852655IndividualAccepts Medicare
Specialties, Licenses & Credentials
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2009
Research & Publications (20)
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
PMID 19551394·Arch Dermatol Res·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·2009
8-other
Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
PMID 18805827·J Med Genet·2009
8-other
How to establish a successful revolving drug fund: the experience of Khartoum state in the Sudan.
PMID 19274366·Bull World Health Organ·2009
8-other
First report of chikungunya from the Maldives.
PMID 18930301·Trans R Soc Trop Med Hyg·2009
7-preclinical
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum Genet·2008
8-other
Spatiotemporal organization of pre-mRNA splicing proteins in plants.
PMID 18630749·Curr Top Microbiol Immunol·2008
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 837 Brown Trl
Bedford, TX 76022 - Phone
- (817) 702-1100
Quick Facts
- NPI
- 1063852655
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 17
- Publications
- 20
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