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GAYLE NORBURY, PH.D.
PH.D.
Group Psychotherapy Psychologist
NPI: 1356489926Individual
Specialties, Licenses & Credentials
Group Psychotherapy PsychologistPrimary
Psychologist — Group Psychotherapy
Code: 103TP2701X
46752(MS)
Research & Publications (15)
Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia.
PMID 19538517·Clin Genet·2009
8-other
Apert syndrome: the current role of prenatal ultrasound and genetic analysis in diagnosis and counselling.
PMID 19077386·Fetal Diagn Ther·2008
5-case
What is the clinical utility of DNA testing in patients with familial hypercholesterolaemia?
PMID 18607183·Curr Opin Lipidol·2008
6-review
Non-invasive prenatal diagnosis of single gene disorders: how close are we?
PMID 18234572·Semin Fetal Neonatal Med·2008
6-review
A functional mutation in the LDLR promoter (-139C>G) in a patient with familial hypercholesterolemia.
PMID 17625505·Eur J Hum Genet·2007
5-case
Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia.
PMID 17539906·Clin Genet·2007
8-other
Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry.
PMID 17181544·Ann Hum Genet·2007
8-other
Novel phenotype of craniosynostosis and ocular anterior chamber dysgenesis with a fibroblast growth factor receptor 2 mutation.
PMID 16158432·Am J Med Genet A·2005
5-case
Ectoparasite and hemoparasite infection in a diverse temperate lizard assemblage at Macraes Flat, South Island, New Zealand.
PMID 15715216·J Parasitol·2004
7-preclinical
Homozygous hypercholesterolaemia and ezetimibe: a case report.
PMID 15046291·Acta Paediatr·2004
5-case
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.
PMID 14564217·Clin Dysmorphol·2003
5-case
Immunological and genetic analysis of 65 patients with a clinical suspicion of X linked hyper-IgM.
PMID 14514918·Mol Pathol·2003
8-other
Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.
PMID 11896626·Oncogene·2002
3-trial
Cystic fibrosis: a further case of an asymptomatic compound heterozygote.
PMID 11746017·Am J Med Genet·2001
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
- 605 STADIUM DRIVE
HATTIESBURG, MS 39401 - Phone
- (601) 450-0310
Quick Facts
- NPI
- 1356489926
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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