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DEBRA MOWAT, MA PHD LMHC
MA PHD LMHC
Mental Health Counselor
NPI: 1477854792Individual
Specialties, Licenses & Credentials
Mental Health CounselorPrimary
Counselor — Mental Health
Code: 101YM0800X
LH 60163793(WA)
Research & Publications (20)
Ethical, legal and social issues surrounding the human genome project.
PMID 11885849·Intern Med J·2002
8-other
Breast cancer risk is not increased in individuals with TWIST1 mutation confirmed Saethre-Chotzen syndrome: an Australian multicenter study.
PMID 19373776·Genes Chromosomes Cancer·2009
4-observational
Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy.
PMID 19026398·Am J Hum Genet·2008
8-other
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
PMID 18825676·Ann Neurol·2008
8-other
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
PMID 18642388·Hum Mutat·2008
8-other
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
PMID 18541964·Clin Dysmorphol·2008
8-other
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
PMID 18252223·Am J Hum Genet·2008
8-other
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy.
PMID 17259292·J Med Genet·2007
8-other
Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesion.
PMID 17107531·Australas Radiol·2006
5-case
Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.
PMID 17100991·Clin Genet·2006
5-case
Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation.
PMID 16088920·Am J Med Genet A·2005
5-case
Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutation.
PMID 16007608·Am J Med Genet A·2005
5-case
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review.
PMID 15908750·Horm Res·2005
5-case
The fast track day hospital: improved care of patients with dementia and associated behavioural disorder.
PMID 15799074·Int J Geriatr Psychiatry·2005
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
- 11502 NE 20TH ST
BELLEVUE, WA 98004 - Phone
- (425) 785-9362
Quick Facts
- NPI
- 1477854792
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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