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WILLIAM SELTZER, PH.D., F.A.C.M.G.
PH.D., F.A.C.M.G.
Ph.D. Medical Genetics
NPI: 1649485616Individual
Specialties, Licenses & Credentials
Ph.D. Medical GeneticsPrimary
Medical Genetics, Ph.D. Medical Genetics
Code: 170100000X
SELTW1(NY)25MS00007900(NJ)1052CLS(MT)DRN00000038(CA)
Research & Publications (20)
The demographic impact of Partition in the Punjab in 1947.
PMID 18587692·Popul Stud (Camb)·2008
8-other
Biochemical markers in persons with preclinical familial Alzheimer disease.
PMID 18509095·Neurology·2008
8-other
A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.
PMID 17666888·Genet Med·2007
4-observational
Rare myelin protein zero sequence variant in late onset CMT1B.
PMID 17602703·J Neurol Sci·2007
8-other
Possible anticipation in hereditary spastic paraplegia type 4 (SPG4).
PMID 17598599·Can J Neurol Sci·2007
5-case
Huntington's Disease-like 2 (HDL2) in North America and Japan.
PMID 15468075·Ann Neurol·2004
4-observational
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis.
PMID 15159497·Neurology·2004
5-case
Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
PMID 15152344·Am J Hum Genet·2004
4-observational
Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes.
PMID 14506936·Amyotroph Lateral Scler Other Motor Neuron Disord·2003
5-case
Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.
PMID 12490063·Genet Test·2002
8-other
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes.
PMID 12207932·Neuromuscul Disord·2002
8-other
A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families.
PMID 11710891·JAMA·2001
8-other
Tales full of sound and fury: a cultural approach to family therapeutic work and research in rural Scandinavia.
PMID 11008649·Fam Process·2000
8-other
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
PMID 10993999·Neurology·2000
5-case
Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G-->C), W44X(G-->A)] in the connexin 32 gene.
PMID 10894999·Eur Neurol·2000
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
- 111 W 3RD AVE, APT. 305
SAN MATEO, CA 94402 - Phone
- (508) 277-7547
Quick Facts
- NPI
- 1649485616
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 1
- Publications
- 20
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