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DAVID EVERMAN, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1659362390Individual
Specialties, Licenses & Credentials
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
21778(SC)
Research & Publications (16)
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
PMID 16761290·Am J Med Genet A·2006
8-other
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
PMID 18660473·J Child Neurol·2008
5-case
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.
PMID 17655765·BMC Med Genet·2007
5-case
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.
PMID 17569090·Hum Genet·2007
4-observational
Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.
PMID 16691619·Am J Med Genet A·2006
8-other
Autosomal dominant inheritance of infantile myofibromatosis.
PMID 15054839·Am J Med Genet A·2004
4-observational
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
PMID 12913067·Hum Mol Genet·2003
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
- 14 EDGEWOOD DR
GREENVILLE, SC 29605 - Phone
- (864) 250-7944
Quick Facts
- NPI
- 1659362390
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 16
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