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MATTHEW FRIEZ, MD
MD
Anatomic Pathology & Clinical Pathology Physician
NPI: 1447442165IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
N5060(TX)
Education
UNIVERSITY OF TEXAS MEDICAL SCHOOL AT HOUSTON
Class of 2005
Research & Publications (20)
Phenotype and genotype in mucolipidoses II and III alpha/beta: a study of 61 probands.
PMID 19617216·J Med Genet·2010
8-other
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.
PMID 18805826·J Med Genet·2009
8-other
Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.
PMID 19610084·Am J Med Genet A·2009
5-case
Hypothesis: dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders.
PMID 18698615·Am J Med Genet A·2008
6-review
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.
PMID 18385275·Genome Res·2008
8-other
Novel FGFR3 mutations in exon 7 and implications for expanded screening of achondroplasia and hypochondroplasia: a response to Heuertz et al.
PMID 17895900·Eur J Hum Genet·2008
8-other
Mediator links epigenetic silencing of neuronal gene expression with x-linked mental retardation.
PMID 18691967·Mol Cell·2008
8-other
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 gene.
PMID 18973276·Am J Med Genet A·2008
8-other
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.
PMID 17369503·J Med Genet·2007
4-observational
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.
PMID 17334363·Nat Genet·2007
8-other
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.
PMID 16909387·Am J Hum Genet·2006
8-other
Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.
PMID 17088400·Pediatrics·2006
8-other
A previously unreported mutation in a Currarino syndrome kindred.
PMID 16906559·Am J Med Genet A·2006
5-case
Early progressive encephalopathy in boys and MECP2 mutations.
PMID 16832102·Neurology·2006
4-observational
Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 gene.
PMID 16353258·Am J Med Genet A·2006
8-other
Parkinsonism, dysautonomia, and intranuclear inclusions in a fragile X carrier: a clinical-pathological study.
PMID 16250026·Mov Disord·2006
5-case
Genetically characterized positive control cell lines derived from residual clinical blood samples.
PMID 16166172·Clin Chem·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2200 W. ILLINOIS AVE
MIDLAND, TX 79707 - Phone
- (432) 683-3206
Quick Facts
- NPI
- 1447442165
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 21
- Publications
- 20
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